Inhibitors of 11-beta-hydroxysteroid dehydrogenase type 1

ABSTRACT

The present invention relates to thiazolinones and also to pharmaceutical compositions comprising the compounds, as well as methods of use of the compounds for treatment of disorders associated with human 11-β-hydroxysteroid dehydrogenase type 1 enzyme and for the preparation of a medicament which acts on the human 11-β-hydroxysteroid dehydrogenase type 1 enzyme.

FIELD OF THE INVENTION

This regular U.S. utility application claims priority to U.S. provisional application Ser. No. 60/775,975, which was filed on Nov. 22, 2005, and which is incorporated herein by reference in its entirety

BACKGROUND OF THE INVENTION

The present invention relates to novel compounds, to pharmaceutical compositions comprising the compounds, as well as to the use of the compounds in medicine and for the preparation of a medicament which acts on the human 11-β-hydroxysteroid dehydrogenase type 1 enzyme (11βHSD1).

Hydroxysteroid dehydrogenases (HSDs) regulate the occupancy and activation of steroid hormone receptors by converting steroid hormones into their inactive metabolites. For a recent review, see Nobel et al., Eur. J. Biochem. 2001, 268:4113-4125.

There exist numerous classes of HSDs. The 11-beta-hydroxysteroid dehydrogenases (11β-HSDs) catalyze the interconversion of active glucocorticoids (such as cortisol and corticosterone), and their inert forms (such as cortisone and 11-dehydrocorticosterone). The isoform 11-beta-hydroxysteroid dehydrogenase type 1 (11β-HSD1) is expressed in liver, adipose tissue, brain, lung and other glucocorticoid tissue and is a potential target for therapy directed at numerous disorders that may be ameliorated by reduction of glucocorticoid action, such as diabetes, obesity and age-related cognitive dysfunction. Seckl, et al., Endocrinology, 2001, 142:1371-1376.

The various isozymes of the 17-beta-hydroxysteroid dehydrogenases (17-βHSDs) bind to androgen receptors or estrogen receptors and catalyze the interconversion of various sex hormones including estradiol/estrone and testosterone/androstenedione. To date, six isozymes have been identified in humans and are expressed in various human tissues including endometrial tissue, breast tissue, colon tissue, and in the testes. 17-beta-Hydroxysteroid dehydrogenase type 2 (17β-HSD2) is expressed in human endometrium and its activity has been reported to be linked to cervical cancer. Kitawaki et al., J. Clin. Endocrin. Metab., 2000, 85:1371-3292-3296. 17-beta-Hydroxysteroid dehydrogenase type 3 (17β-HSD3) is expressed in the testes and its modulation may be useful for the treatment of androgen-related disorders.

Androgens and estrogens are active in their 17β-hydroxy configurations, whereas their 17-keto derivatives do not bind to androgen and estrogen receptors and are thus inactive. The conversion between the active and inactive forms (estradiol/estrone and testosterone/androstenedione) of sex hormones is catalyzed by members of the 17β-HSD family. 17β-HSD1 catalyzes the formation of estradiol in breast tissue, which is important for the growth of malignant breast tumors. Labrie et al., Mol. Cell. Endocrinol. 1991, 78:C113-C118. A similar role has been suggested for 17β-HSD4 in colon cancer. English et al., J. Clin. Endocrinol. Metab. 1999, 84:2080-2085. 17β-HSD3 is almost exclusively expressed in the testes and converts androstenedione into testosterone. Deficiency of this enzyme during fetal development leads to male pseudohermaphroditism. Geissler et al., Nat. Genet. 1994, 7:34-39. Both 17β-HSD3 and various 3α-HSD isozymes are involved in complex metabolic pathways which lead to androgen shuffles between inactive and active forms. Penning et al., Biochem. J. 2000, 351:67-77. Thus, modulation of certain HSDs can have potentially beneficial effects in the treatment of androgen- and estrogen-related disorders.

The 20-alpha-hydroxysteroid dehydrogenases (20α-HSDs) catalyze the interconversion of progestins (such as between progesterone and 20α-hydroxy progesterone). Other substrates for 20α-HSDs include 17α-hydroxypregnenolone or 17α-hydroxyprogesterone, leading to 20α-OH steroids. Several 20α-HSD isoforms have been identified and 20α-HSDs are expressed in various tissues, including the placenta, ovaries, testes and adrenals. Peltoketo, et al., J. Mol. Endocrinol. 1999, 23:1-11.

The 3-alpha-hydroxysteroid dehydrogenases (3α-HSDs) catalyze the interconversion of the androgens dihydrotestosterone (DHT) and 5αandrostane-3α,17β-diol and the interconversion of the androgens DHEA and androstenedione and therefore play an important role in androgen metabolism. Ge et al., Biology of Reproduction 1999, 60:855-860.

1. Glucorticoids, Diabetes and Hepatic Glucose Production

It has been known for more than half a century that glucocorticoids have a central role in diabetes. For example, the removal of the pituitary gland or the adrenal gland from a diabetic animal alleviates the most severe symptoms of diabetes and lowers the concentration of glucose in the blood (Long, C. D. and Leukins, F. D. W. (1936) J. Exp. Med. 63: 465-490; Houssay, B. A. (1942) Endocrinology 30: 884-892). It is also well established that glucocorticoids enable the effect of glucagon on the liver.

The role of 11βHSD1 as an important regulator of local glucocorticoid effect and thus of hepatic glucose production is well substantiated (see, e.g., Jamieson et al. (2000) J. Endocrinol. 165: 685-692). Hepatic insulin sensitivity was improved in healthy human volunteers treated with the non-specific 11βHSD1 inhibitor carbenoxolone (Walker, B. R. et al. (1995) J. Clin. Endocrinol. Metab. 80: 3155-3159). Furthermore, the expected mechanism has been established by different experiments with mice and rats. These studies showed that the mRNA levels and activities of two key enzymes in hepatic glucose production were reduced, namely: the rate-limiting enzyme in gluconeogenesis, phosphoenolpyruvate carboxykinase (PEPCK), and glucose-6-phosphatase (G6Pase) the enzyme catalyzing the last common step of gluconeogenesis and glycogenolysis. Finally, blood glucose levels and hepatic glucose production are reduced in mice in which the 11βHSD1 gene is knocked-out. Data from this model also confirm that inhibition of 11βHSD1 will not cause hypoglycemia, as predicted since the basal levels of PEPCK and G6Pase are regulated independently of glucocorticoids (Kotelevtsev, Y. et al., (1997) Proc. Natl. Acad. Sci. USA 94:14924-14929).

FR 2,384,498 discloses compounds having a high hypoglycemic effect. Therefore, treatment of hyperglycemia with these compounds may lead to hypoglycemia.

2. Reduction of Obesity and Obesity Related Cardiovascular Risk Factors

Obesity is an important factor in syndrome X as well as in the majority (>80%) of type 2 diabetes, and omental fat appears to be of central importance. Abdominal obesity is closely associated with glucose intolerance, hyperinsulinemia, hypertriglyceridemia, and other factors of the so-called syndrome X (e.g. increased blood pressure, decreased levels of HDL and increased levels of VLDL) (Montague & O'Rahilly, Diabetes 49: 883-888, 2000). Inhibition of the 11βHSD1 enzyme in pre-adipocytes (stromal cells) has been shown to decrease the rate of differentiation into adipocytes. This is predicted to result in diminished expansion (possibly reduction) of the omental fat depot, i.e., reduced central obesity (Bujalska, I. J., S. Kumar, and P. M. Stewart (1997) Lancet 349: 1210-1213).

Inhibition of 11βHSD1 in mature adipocytes is expected to attenuate secretion of the plasminogen activator inhibitor 1 (PAI-1)- an independent cardiovascular risk factor (Halleux, C. M. et al. (1999) J. Clin. Endocrinol. Metab. 84: 4097-4105). Furthermore, there is a clear correlation between glucocorticoid “activity” and cardiovascular risk factor suggesting that a reduction of the glucocorticoid effects would be beneficial (Walker, B. R. et al. (1998) Hypertension 31: 891-895; Fraser, R. et al. (1999) Hypertension 33: 1364-1368).

Adrenalectomy attenuates the effect of fasting to increase both food intake and hypothalamic neuropeptide Y expression. This supports the role of glucocorticoids in promoting food intake and suggests that inhibition of 11βHSD1 in the brain might increase satiety and therefore reduce food intake (Woods, S. C. et al. (1998) Science, 280: 1378-1383).

3. Beneficial Effect on the Pancreas

Inhibition of 11βHSD1 in isolated murine pancreatic β-cells improves glucose-stimulated insulin secretion (Davani, B. et al. (2000) J. Biol. Chem. 2000 Nov. 10; 275(45): 34841-4). Glucocorticoids were previously known to reduce pancreatic insulin release in vivo (Billaudel, B. and B. C. J. Sutter (1979) Horm. Metab. Res. 11: 555-560). Thus, inhibition of 11βHSD1 is predicted to yield other beneficial effects for diabetes treatment, besides the effects on liver and fat.

4. Beneficial Effects on Cognition and Dementia

Stress and glucocorticoids influence cognitive function (de Quervain, D. J.-F., B. Roozendaal, and J. L. McGaugh (1998) Nature 394: 787-790). The enzyme 11βHSD1 controls the level of glucocorticoid action in the brain and thus contributes to neurotoxicity (Rajan, V., C. R. W. Edwards, and J. R. Seckl, J. (1996) Neuroscience 16: 65-70; Seckl, J. R., Front. (2000) Neuroendocrinol. 18: 49-99). Unpublished results indicate significant memory improvement in rats treated with a non-specific 11βHSD1 inhibitor (J. Seckl, personal communication). Based the above and on the known effects of glucocorticoids in the brain, it may also be suggested that inhibiting 11βHSD1 in the brain may result in reduced anxiety (Tronche, F. et al. (1999) Nature Genetics 23: 99-103). Thus, taken together, the hypothesis is that inhibition of 11βHSD1 in the human brain would prevent reactivation of cortisone into cortisol and protect against deleterious glucocorticoid-mediated effects on neuronal survival and other aspects of neuronal function, including cognitive impairment, depression, and increased appetite.

5. Use of Immuno-Modulation Using 11βHSD1 Inhibitors

The general perception is that glucocorticoids suppress the immune system. But in fact there is a dynamic interaction between the immune system and the HPA (hypothalamo-pituitary-adrenal) axis (Rook, G. A. W. (1999) Baillièr's Clin. Endocrinol. Metab. 13: 576-581). The balance between the cell-mediated response and humoral responses is modulated by glucocorticoids. A high glucocorticoid activity, such as at a state of stress, is associated with a humoral response. Thus, inhibition of the enzyme 11βHSD1 has been suggested as a means of shifting the response towards a cell-based reaction.

In certain disease states, including tuberculosis, lepra and psoriasis the immune reaction is normally biased towards a humoral response when in fact the appropriate response would be cell based. Temporal inhibition of 11βHSD1, local or systemic, might be used to push the immune system into the appropriate response (Mason, D. (1991) Immunology Today 12: 57-60; Rook et al., supra).

An analogous use of 11βHSD1 inhibition, in this case temporal, would be to booster the immune response in association with immunization to ensure that a cell based response would be obtained, when desired.

6. Reduction of Intraocular Pressure

Recent data suggest that the levels of the glucocorticoid target receptors and the 11βHSD enzymes determines the susceptibility to glaucoma (Stokes, J. et al. (2000) Invest. Ophthalmol. 41: 1629-1638). Further, inhibition of 11βHSD1 was recently presented as a novel approach to lower the intraocular pressure (Walker E. A. et al, poster P3-698 at the Endocrine society meeting Jun. 12-15, 1999, San Diego). Ingestion of carbenoxolone, a non-specific inhibitor of 11βHSD1, was shown to reduce the intraocular pressure by 20% in normal subjects. In the eye, expression of 11βHSD1 is confined to basal cells of the corneal epithelium and the non-pigmented epithelialium of the cornea (the site of aqueous production), to ciliary muscle and to the sphincter and dilator muscles of the iris. In contrast, the distant isoenzyme 11βHSD2 is highly expressed in the non-pigmented ciliary epithelium and corneal endothelium. None of the enzymes is found at the trabecular meshwork, the site of drainage. Thus, 11βHSD1 is suggested to have a role in aqueous production, rather than drainage, but it is presently unknown if this is by interfering with activation of the glucocorticoid or the mineralocorticoid receptor, or both.

7. Reduced Osteoporosis

Glucocorticoids have an essential role in skeletal development and function but are detrimental in excess. Glucocorticoid-induced bone loss is derived, at least in part, via inhibition of bone formation, which includes suppression of osteoblast proliferation and collagen synthesis (Kim, C. H., Cheng, S. L. and Kim, G. S. (1999) J. Endocrinol. 162: 371-379). The negative effect on bone nodule formation could be blocked by the non-specific inhibitor carbenoxolone suggesting an important role of 11βHSD1 in the glucocorticoid effect (Bellows, C. G., Ciaccia, A. and Heersche, J. N. M. (1998) Bone 23: 119-125). Other data suggest a role of 11βHSD1 in providing sufficiently high levels of active glucocorticoid in osteoclasts, and thus in augmenting bone resorption (Cooper, M. S. et al. (2000) Bone 27: 375-381). Taken together, these different data suggest that inhibition of 11βHSD1 may have beneficial effects against osteoporosis by more than one mechanism working in parallel.

8. Reduction of Hypertension

Bile acids inhibit 11β-hydroxysteroid dehydrogenase type 2. This results in a shift in the overall body balance in favour of cortisol over cortisone, as shown by studying the ratio of the urinary metabolites (Quattropani, C., Vogt, B., Odermatt, A., Dick, B., Frey, B. M., Frey, F. J. (2001) J Clin Invest. November; 108(9):1299-305. “Reduced activity of 11beta-hydroxysteroid dehydrogenase in patients with cholestasis”.). Reducing the activity of 11bHSD1 in the liver by a selective inhibitor is predicted to reverse this imbalance, and acutely counter the symptoms such as hypertension, while awaiting surgical treatment removing the biliary obstruction.

WO 99/65884 discloses carbon substituted aminothiazole inhibitors of cyclin dependent kinases. These compounds may, e.g., be used against cancer, inflammation and arthritis. U.S. Pat. No. 5,856,347 discloses an antibacterial preparation or bactericide comprising 2-aminothiazole derivative and/or salt thereof. Further, U.S. Pat. No. 5,403,857 discloses benzenesulfonamide derivatives having 5-lipoxygenase inhibitory activity. Additionally, tetrahydrothiazolo[5,4-c]pyridines are disclosed in: Analgesic tetrahydrothiazolo[5,4-c]pyridines. Fr. Addn. (1969), 18 pp, Addn. to Fr. 1498465. CODEN: FAXXA3; FR 94123 19690704 CAN 72:100685 AN 1970:100685 CAPLUS and 4,5,6,7-Tetrahydrothiazolo[5,4-c]pyridines. Neth. Appl. (1967), 39 pp. CODEN: NAXXAN NL 6610324 19670124 CAN 68:49593, AN 1968: 49593 CAPLUS. However, none of the above disclosures discloses the compounds according to the present invention, or their use for the treatment of diabetes, obesity, glaucoma, osteoporosis, cognitive disorders, immune disorders, depression, and hypertension.

WO 98/16520 discloses compounds inhibiting matrix metalloproteinases (MMPs) and TNF-α converting enzyme (TACE). EP 0 749 964 A1 and U.S. Pat. No. 5,962,490 disclose compounds having an endothelin receptor antagonist activity. WO 00/02851 discloses compounds associated with a disturbed cGMP balance. None of these compounds fall within the present invention. Furthermore, nothing is said about the activity on 11βHSD1.

U.S. Pat. No. 5,783,697 discloses thiophene derivatives as inhibitors of PGE2 and LTB4. Nothing is said about the activity on 11βHSD1.

EP 0 558 258, EP 0 569 193, and EP 1 069 114 disclose isoxazole derivatives as endothelin agonists and antagonists. Nothing is said about the activity on 11βHSD1.

9. Wound Healing

Cortisol performs a broad range of metabolic functions and other functions. The multitude of glucocorticoid action is exemplified in patients with prolonged increase in plasma glucocorticoids, so called “Cushing's syndrome”. Patients with Cushing's syndrome have prolonged increase in plasma glucocorticoids and exhibit impaired glucose tolerance, type 2 diabetes, central obesity, and osteoporosis. These patients also have impaired wound healing and brittle skin (Ganong, W. F. Review of Medical Physiology. Eighteenth edition ed. Stamford, Conn.: Appleton & Lange; 1997).

Glucocorticoids have been shown to increase risk of infection and delay healing of open wounds (Anstead, G. M. Steroids, retinoids, and wound healing. Adv Wound Care 1998; 11(6):277-85). Patients treated with glucocorticoids have 2-5-fold increased risk of complications when undergoing surgery (Diethelm, A. G. Surgical management of complications of steroid therapy. Ann Surg 1977; 185(3):251-63).

The European patent application No. EP 0902288 discloses a method for diagnosing the status of wound healing in a patient, comprising detecting cortisol levels in said wound. The authors suggest that elevated levels of cortisol in wound fluid, relative to normal plasma levels in healthy individuals, correlates with large, non-healing wounds (Hutchinson, T. C., Swaniker, H. P., Wound diagnosis by quantitating cortisol in wound fluids. European patent application No. EP 0 902 288, published Mar. 17, 1999).

In humans, the 11β-HSD catalyzes the conversion of cortisol to cortisone, and vice versa. The parallel function of 11β-HSD in rodents is the interconversion of corticosterone and 11-dehydrocorticosterone (Frey, F. J., Escher, G., Frey, B. M. Pharmacology of 11 beta-hydroxysteroid dehydrogenase. Steroids 1994; 59(2):74-9). Two isoenzymes of 11β-HSD, 11β-HSD1 and 11β-HSD2, have been characterized, and differ from each other in function and tissue distribution (Albiston, A. L., Obeyesekere, V. R., Smith, R. E., Krozowski, Z. S. Cloning and tissue distribution of the human 11 beta-hydroxysteroid dehydrogenase type 2 enzyme. Mol Cell Endocrinol 1994; 105(2):R11-7). Like GR, 11β-HSD1 is expressed in numerous tissues like liver, adipose tissue, adrenal cortex, gonads, lung, pituitary, brain, eye etc. (Monder C, White P C. 11 beta-hydroxysteroid dehydrogenase. Vitam Horm 1993; 47:187-271; Stewart, P. M., Krozowski, Z. S. 11 beta-Hydroxysteroid dehydrogenase. Vitam Horm 1999; 57:249-324; Stokes, J., Noble, J., Brett, L., Phillips, C., Seckl, J. R., O'Brien, C., et al. Distribution of glucocorticoid and mineralocorticoid receptors and 11beta-hydroxysteroid dehydrogenases in human and rat ocular tissues. Invest Ophthalmol Vis Sci 2000; 41(7):1629-38). The function of 11β-HSD1 is to fine-tune local glucocorticoid action. 11β-HSD activity has been shown in the skin of humans and rodents, in human fibroblasts and in rat skin pouch tissue (Hammami, M. M., Siiteri, P. K. Regulation of 11 beta-hydroxysteroid dehydrogenase activity in human skin fibroblasts: enzymatic modulation of glucocorticoid action. J Clin Endocrinol Metab 1991; 73(2):326-34); Cooper, M. S., Moore, J., Filer, A., Buckley, C. D., Hewison, M., Stewart, P. M. 11beta-hydroxysteroid dehydrogenase in human fibroblasts: expression and regulation depends on tissue of origin. ENDO 2003 Abstracts 2003; Teelucksingh, S., Mackie, A. D., Burt, D., McIntyre, M. A., Brett, L., Edwards, C. R. Potentiation of hydrocortisone activity in skin by glycyrrhetinic acid. Lancet 1990; 335(8697):1060-3; Slight, S. H., Chilakamarri, V. K., Nasr, S., Dhalla, A. K., Ramires, F. J., Sun, Y., et al. Inhibition of tissue repair by spironolactone: role of mineralocorticoids in fibrous tissue formation. Mol Cell Biochem 1998; 189(1-2):47-54).

Wound healing consists of serial events including inflammation, fibroblast proliferation, secretion of ground substances, collagen production, angiogenesis, wound contraction and epithelialization. It can be divided in three phases; inflammatory, proliferative and remodeling phase (reviewed in Anstead et al., supra).

In surgical patients, treatment with glucocorticoids increases risk of wound infection and delay healing of open wounds. It has been shown in animal models that restraint stress slows down cutaneous wound healing and increases susceptibility to bacterial infection during wound healing. These effects were reversed by treatment with the glucocorticoid receptor antagonist RU486 (Mercado, A. M., Quan, N., Padgett, D. A., Sheridan, J. F., Marucha, P. T. Restraint stress alters the expression of interleukin-1 and keratinocyte growth factor at the wound site: an in situ hybridization study. J Neuroimmunol 2002; 129(1-2):74-83; Rojas, I. G., Padgett, D. A., Sheridan, J. F., Marucha, P. T. Stress-induced susceptibility to bacterial infection during cutaneous wound healing. Brain Behav Immun 2002; 16(1):74-84). Glucocorticoids produce these effects by suppressing inflammation, decrease wound strength, inhibit wound contracture and delay epithelialization (Anstead et al., supra). Glucocorticoids influence wound healing by interfering with production or action of cytokines and growth factors like IGF, TGF-β, EGF, KGF and PDGF (Beer, H. D., Fassler, R., Werner, S. Glucocorticoid-regulated gene expression during cutaneous wound repair. Vitam Horm 2000; 59:217-39; Hamon, G. A., Hunt, T. K., Spencer, E. M. In vivo effects of systemic insulin-like growth factor-I alone and complexed with insulin-like growth factor binding protein-3 on corticosteroid suppressed wounds. Growth Regul 1993; 3(1):53-6; Laato, M., Heino, J., Kahari, V. M., Niinikoski, J., Gerdin, B. Epidermal growth factor (EGF) prevents methylprednisolone-induced inhibition of wound healing. J Surg Res 1989; 47(4):354-9; Pierce, G. F., Mustoe, T. A., Lingelbach, J., Masakowski, V. R., Gramates, P., Deuel, T. F. Transforming growth factor beta reverses the glucocorticoid-induced wound-healing deficit in rats: possible regulation in macrophages by platelet-derived growth factor. Proc Natl Acad Sci USA 1989; 86(7):2229-33). It has also been shown that glucocorticoids decrease collagen synthesis in rat and mouse skin in vivo and in rat and human fibroblasts (Oishi, Y., Fu, Z. W., Ohnuki, Y., Kato, H., Noguchi, T. Molecular basis of the alteration in skin collagen metabolism in response to in vivo dexamethasone treatment: effects on the synthesis of collagen type I and III, collagenase, and tissue inhibitors of metalloproteinases. Br J Dermatol 2002; 147(5):859-68).

WO 01/90090 discloses thiazole compounds, which compounds inhibit the human 11β-HSD1, and may be useful for treating disorders such as diabetes, obesity, glaucoma, osteoporosis, cognitive disorders and immune disorders. Other 11β-HSD1 inhibitors are disclosed in e.g. WO 01/90091; WO 01/90092; WO 01/90093; WO 01/90094; WO 03/043999; WO 03/044000; WO 03/044009; U.S. Patent Publication No. 2005/009821; WO 04/103980; WO 04/112784; WO 04/112781; WO 04/112785; WO 04/112783; WO 04/112782; WO 04/113310; WO 04/112779; and Swedish patent application No. SE 0400227-5, filed on Feb. 4, 2004. However, the use of the 11β-HSD1 inhibitors according to the present invention for diabetes, obesity, glaucoma, osteoporosis, cognitive disorders, immune disorders, and wound healing has not previously been disclosed.

Although not disclosed as 11β-HSD1 inhibitors, Okawara et al. disclose the preparation of thiazole-5-spiropropan-4(5H)-ones, see J. Chem. Soc. Perkin Trans. I, 1733-1735 (1986).

SUMMARY OF THE INVENTION

The compounds according to the present invention solve the above problems and embrace a novel class of compounds that has been developed and that inhibits the human 11-β-hydroxysteroid dehydrogenase type 1 enzyme (11-β-HSD1), and may therefore be of use in treating disorders related to 11-β-HSD1 activity, such as, but not limited to diabetes, obesity, glaucoma, osteoporosis, cognitive disorders, immune disorders, hypertension, and wound healing.

One embodiment of the present invention is a compound selected from the group consisting of:

One embodiment relates to a pharmaceutical formulation comprising a compound of the invention as active ingredient, in combination with a pharmaceutically acceptable diluent or carrier.

In one embodiment, the pharmaceutical formulation is formulated for oral delivery.

In one embodiment, the oral delivery form is a tablet.

One embodiment relates to a method for the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or achieving immuno-modulation comprising administering the compound of the invention to an individual.

In one embodiment, the disorder is selected from diabetes, syndrome X, obesity, glaucoma, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, dementia, depression, virus diseases, and inflammatory diseases.

Another embodiment relates to the treatment or prophylaxis of a medical condition involving delayed or impaired wound healing.

Another embodiment relates to methods of treatment wherein the medical condition involving delayed or impaired wound healing is diabetes.

Another embodiment relates to methods of treatment wherein the medical condition involving delayed or impaired wound healing is caused by treatment with glucocorticoids.

Another embodiment relates to methods of treatment for the promotion of wound healing in chronic wounds, such as diabetic ulcers, venous ulcers or pressure ulcers.

Another embodiment relates to methods of treatment wherein immuno-modulation is selected from tuberculosis, lepra, and psoriasis.

Another embodiment relates to a method for inhibiting a 11-β-hydroxysteroid dehydrogenase type 1 enzyme, which comprises administering to a subject in need of such treatment an effective amount of a compound of the invention.

When using the compounds of the invention in therapy (e.g., Examples 39, 67, and 69-72), they may advantageously be used in the prophylaxis or treatment of an 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or achieving immuno-modulation. In this embodiment, the disorder may be selected from diabetes, syndrome X, obesity, glaucoma, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, dementia, depression, virus diseases, and inflammatory diseases. It is also possible that the treatment or prophylaxis is of the medical condition involves delayed or impaired wound healing. The medical condition involving delayed or impaired wound healing may be associated with diabetes and may have been caused by treatment with glucocorticoids. The compounds of the invention for use in therapy may be for promotion of wound healing in chronic wounds, such as diabetic ulcers, venous ulcers or pressure ulcers. immuno-modulation may encompass tuberculosis, lepra, and psoriasis.

Another embodiment of the present invention is a pharmaceutical formulation comprising a compound of the invention for use in therapy as active ingredient, in combination with a pharmaceutically acceptable diluent or carrier, especially for use in the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or achieving immuno-modulation. The pharmaceutical formulation can include a second active ingredient. The second active ingredient can be an inhibitor of 11-β-hydroxysteroid dehydrogenase type 1 or it can have some other activity.

Another embodiment of the present invention is a method for the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or achieving immuno-modulation, which comprises administering to a subject in need of such treatment an effective amount of a compound of the invention.

Another embodiment of the present invention is a method for inhibiting a 11-β-hydroxysteroid dehydrogenase type 1 enzyme, which comprises administering to a subject in need of such treatment an effective amount of a compound of the invention.

Another embodiment of the present invention is the use of a compound of the invention, for the manufacture of a medicament for use in the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or achieving immuno-modulation.

Examples of 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorders include: diabetes, syndrome X, obesity, glaucoma, osteoporosis, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, cognitive disorders, dementia, depression, immune disorders, virus diseases, wound healing and inflammatory diseases.

Illustrative medical conditions involving delayed or impaired wound healing include but are not limited to diabetes.

Illustrative medical conditions involving delayed or impaired wound healing include but are not to medical conditions caused by treatment with glucocorticoids.

The compound of the invention may be used for the promotion of wound healing in chronic wounds, such as diabetic ulcers, venous ulcers or pressure ulcers.

Illustrative immuno-modulations include but are not limited to tuberculosis, lepra, and psoriasis.

Also, within the scope of this invention is a method for making a compound of the invention. The method includes taking any intermediate compound delineated herein, reacting it with one or more reagents to form a compound of the invention, including any processes specifically delineated herein.

Use of a compound of the invention, for the manufacture of a medicament for use in the prophylaxis or treatment of a 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder or achieving immuno-modulation. In one embodiment, the disorder is selected from diabetes, syndrome X, obesity, glaucoma, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, dementia, depression, virus diseases, and inflammatory diseases. In another embodiment, the medical condition involving delayed or impaired wound healing. In another embodiment, the medical condition involving delayed or impaired wound healing is diabetes. In another embodiment, the medical condition involving delayed or impaired wound healing is caused by treatment with glucocorticoids. In another embodiment, the use is for the promotion of wound healing in chronic wounds, such as diabetic ulcers, venous ulcers or pressure ulcers. In another embodiment, the immuno-modulation is selected from tuberculosis, lepra, and psoriasis.

Other features and advantages of the invention will be apparent from the detailed description and claims.

DETAILED DESCRIPTION OF THE INVENTION

The compounds according to the present invention may be used in several indications which involve 11-β-hydroxysteroid dehydrogenase type 1 enzyme. Thus, the compounds according to the present invention may be used against dementia (see WO97/07789), osteoporosis (see Canalis, E. 1996, Mechanisms of glucocorticoid action in bone: implications to glucocorticoid-induced osteoporosis, Journal of Clinical Endocrinology and Metabolism, 81, 3441-3447) and may also be used for disorders in the immune system (see Franchimont et al, “Inhibition of Th1 immune response by glucocorticoids: dexamethasone selectively inhibits IL-12-induced Stat 4 phosphorylation in T lymphocytes”, The journal of Immunology 2000, Feb. 15, vol 164 (4), pages 1768-74) and also in the above listed indications.

The various terms used, separately and in combinations, in the above definition of the compounds of the invention will be explained.

The term “aryl” in the present description is intended to include aromatic rings (monocyclic or bicyclic) having from 6 to 10 ring carbon atoms, such as phenyl (Ph), naphthyl, and indanyl (i. e., 2,3-dihydroindenyl), which optionally may be substituted by C₁₋₆-alkyl. Examples of substituted aryl groups are benzyl, and 2-methylphenyl.

The term “heteroaryl” means in the present description a monocyclic, bi- or tricyclic aromatic ring system (only one ring need to be aromatic) having from 5 to 14, preferably 5 to 10 ring atoms such as 5, 6, 7, 8, 9 or 10 ring atoms (mono- or bicyclic), in which one or more of the ring atoms are other than carbon, such as nitrogen, sulfur, oxygen and selenium as part of the ring system. Examples of such heteroaryl rings are pyrrole, imidazole, thiophene, furan, thiazole, isothiazole, thiadiazole, oxazole, isoxazole, oxadiazole, pyridine, pyrazine, pyrimidine, pyridazine, pyrazole, triazole, tetrazole, chroman, isochroman, quinoline, quinoxaline, isoquinoline, phthalazine, cinnoline, quinazoline, indole, isoindole, benzothiophene, benzofuran, isobenzofuran, benzoxazole, 2,1,3-benzoxadiazole, benzopyrazole; benzothiazole, 2,1,3-benzothiazole, 2,1,3-benzoselenadiazole, benzimidazole, indazole, benzodioxane, indane, 1,5-naphthyridine, 1,8-naphthyridine, acridine, fenazine and xanthene.

The term “heterocyclic” and “heterocyclyl” in the present description is intended to include unsaturated as well as partially and fully saturated mono-, bi- and tricyclic rings having from 4 to 14, preferably 4 to 10 ring atoms having one or more heteroatoms (e.g., oxygen, sulfur, or nitrogen) as part of the ring system and the reminder being carbon, such as, for example, the heteroaryl groups mentioned above as well as the corresponding partially saturated or fully saturated heterocyclic rings. Exemplary saturated heterocyclic rings are azetidine, pyrrolidine, piperidine, piperazine, morpholine, thiomorpholine, 1,4-oxazepane, azepane, phthalimide, indoline, isoindoline, 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroisoquinoline, 3,4-dihydro-2H-1,4-benzoxazine, hexahydroazepine, 3,4-dihydro-2(1H)isoquinoline, 2,3-dihydro-1H-indole, 1,3-dihydro-2H-isoindole, azocane, 1-oxa-4-azaspiro[4.5]dec-4-ene, decahydroisoquinoline, and 1,4-diazepane. In addition, the heterocyclyl or heterocyclic moiety may optionally be substituted with one or more oxo groups.

C₁₋₈-alkyl in the compound of the invention according to the present application may be a straight or branched alkyl group containing 1-8 carbon atoms. Exemplary alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, isopentyl, hexyl, isohexyl, n-heptyl, and n-octyl. For parts of the range “C₁₋₈-alkyl” all subgroups thereof are contemplated such as C₁₋₇-alkyl, C₁₋₆-alkyl, C₁₋₅-alkyl, C₁₋₄-alkyl, C₂₋₈-alkyl, C₂₋₇-alkyl, C₂₋₆-alkyl, C₂₋₅-alkyl, C₃₋₇-alkyl, C₄₋₆-alkyl, etc.

C₁₋₈-alkoxy in the compound of the invention according to the present application may be a straight or branched alkoxy group containing 1-8 carbon atoms. Exemplary alkoxy groups include methoxy, ethoxy, propoxy, isopropoxy, butoxy, sec-butoxy, tert-butoxy, pentyloxy, isopentyloxy, hexyloxy, isohexyloxy, n-heptyloxy, and n-octyloxy. For parts of the range “C₁₋₆-alkoxy” all subgroups thereof are contemplated such as C₁₋₇-alkoxy, C₁₋₆-alkoxy, C₁₋₅-alkoxy, C₁₋₄-alkoxy, C₂₋₈-alkoxy, C₂₋₇-alkoxy, C₂₋₆-alkoxy, C₂₋₅-alkoxy, C₃₋₇-alkoxy, C₄₋₆-alkoxy, etc.

C₁₋₈-acyl in the compound of the invention according to the present application may be a straight or branched acyl group containing 1-8 carbon atoms. Exemplary acyl groups include formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, n-hexanoyl, n-heptanoyl, and n-octanoyl. For parts of the range “C₁₋₈-acyl” all subgroups thereof are contemplated such as C₁₋₇-acyl, C₁₋₆-acyl, C₁₋₅-acyl, C₁₋₄-acyl, C₂₋₈-acyl, C₂₋₇-acyl, C₂₋₆-acyl, C₂₋₅-acyl, C₃₋₇-acyl, C₄₋₆-acyl, etc.

C₂₋₈-alkenyl in the compound of the invention according to the present application may be a straight or branched acyl group containing 2-8 carbon atoms. Exemplary alkenyl groups include vinyl, 1-propenyl, 2-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 1-pentenyl, 2-pentenyl, 1-hexenyl, 2-hexenyl, 1-heptenyl, and 1-octenyl. For parts of the range “C₂₋₈-alkenyl” all subgroups thereof are contemplated such as C₂₋₇-alkenyl, C₂₋₆-alkenyl, C₂₋₅-alkenyl, C₂₋₄-alkenyl, C₃₋₈-alkenyl, C₃₋₇-alkenyl, C₃₋₆-alkenyl, C₃₋₅-alkenyl, C₄₋₇-alkenyl, C₅₋₆-alkenyl, etc.

C₃₋₁₀-cycloalkyl in the compound of the invention according to the present application may be an optionally substituted monocyclic, bicyclic or tricyclic alkyl group containing between 3-10 carbon atoms. Exemplary cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, bicyclo[2.2.1 ]hept-2-yl, tricyclo[3.3.1.0˜3,7˜]non-3-yl, (1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl, (1S,2S,3S,5R)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl, 1-adamantyl, noradamantyl, and 2,2,3,3-tetramethylcyclopropyl. For parts of the range “C₃₋₁₀-cycloalkyl” all subgroups thereof are contemplated such as C₃₋₉-cycloalkyl, C₃₋₈-cycloalkyl, C₃₋₇-cycloalkyl, C₃₋₆-cycloalkyl, C₃₋₅-cycloalkyl, C₄₋₁₀-cycloalkyl, C₅₋₁₀-cycloalkyl, C₆₋₁₀-cycloalkyl, C₇₋₁₀-cycloalkyl, C₈₋₉-cycloalkyl, etc. In addition, the cycloalkyl moiety may optionally be substituted with one or more oxo groups.

C₃₋₁₀-cycloalkenyl in the compound of the invention according to the present application may be an optionally alkyl substituted cyclic, bicyclic or tricyclic alkenyl group containing totally 3-10 carbon atoms. Exemplary cycloalkenyl groups include cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, cyclononenyl, cyclodecenyl, and bicyclo[2.2.1]hept-5-en-2-yl. For parts of the range “C₃₋₁₀-cycloalkenyl” all subgroups thereof are contemplated such as C₃₋₉-cycloalkenyl, C₃₋₈-cycloalkenyl, C₃₋₇-cycloalkenyl, C₃₋₆-cycloalkenyl, C₃₋₅-cycloalkenyl, C₄₋₁₀-cycloalkenyl, C₅₋₁₀-cycloalkenyl, C₆₋₁₀-cycloalkenyl, C₇₋₁₀-cycloalkenyl, C₈₋₉-cycloalkenyl, etc. In addition, the cycloalkenyl moiety may optionally be substituted with one or more oxo groups.

The term “halogen” or “halo” in the present description is intended to include fluorine, chlorine, bromine and iodine.

The term “sulfanyl” in the present description means a thio group.

The term “-hetero(C₁-C₈)alkyl” refers to a moiety wherein a hetero atom, selected from optionally substituted nitrogen, sulfur and oxygen, is the point of attachment to the core molecule and is attached to a C₁-C₈ alkyl chain.

The term “cyclic amide spiro ring” refers to compounds where the substituents at the 5-position of the thiazolinone or the oxazolone ring combine together to form a cyclic ring having a —NR¹⁰C(O)— therein. An example of such a moiety is shown in the example below:

With the expression “mono- or di-substituted” is meant in the present description that the functionalities in question may be substituted with independently C₁₋₈-acyl, C₂₋₈-alkenyl, C₁₋₈-(cyclo)alkyl, aryl, pyridylmethyl, or heterocyclic rings e.g. azetidine, pyrrolidine, piperidine, piperazine, morpholine and thiomorpholine, which heterocyclic rings optionally may be substituted with C₁₋₈-alkyl. With the expression “optionally mono- or disubstituted” is meant in the present description that the functionalities in question may also be substituted with independently hydrogen.

When two of the above-mentioned terms are used together, it is intended that the latter group is substituted by the former. For example, C₃₋₁₀-cycloalkyl-C₁₋₈-alkyl means a C₁₋₈-alkyl group that is substituted by a C₃₋₁₀-cycloalkyl group. Likewise, a C₁₋₈-haloalkyl means a C₁₋₈-alkyl group that is substituted by a halogen atom.

Metabolites of the compounds of the invention can take on many forms and the present invention encompasses the metabolites of the compounds as well as the parent compound.

As used herein, the term “prodrug” means a derivative of a compound that can hydrolyze, oxidize, or otherwise react under biological conditions (in vitro or in vivo) to provide an active compound, particularly a benzamide derivative. Examples of prodrugs include, but are not limited to, derivatives and metabolites of a benzamide derivative that include biohydrolyzable groups such as biohydrolyzable amides, biohydrolyzable esters, biohydrolyzable carbamates, biohydrolyzable carbonates, biohydrolyzable ureides, and biohydrolyzable phosphate analogues (e.g., monophosphate, diphosphate or triphosphate). Illustrative prodrugs of compounds with carboxyl functional groups include but are not limited to the lower alkyl esters of the carboxylic acid. The carboxylate esters are conveniently formed by esterifying any of the carboxylic acid moieties present on the molecule. Prodrugs can typically be prepared using well-known methods, such as those described by Burger's Medicinal Chemistry and Drug Discovery 6^(th) ed. (Donald J. Abraham ed., 2001, Wiley) and Design and Application of Prodrugs (H. Bundgaard ed., 1985, Harwood Academic Publishers Gmfh).

“Tautomer” is one of two or more structural isomers that exist in equilibrium and are readily converted from one isomeric form to another, in the present case, tautomers of the structures below are encompassed by the present invention.

As used herein, “hydrate” is a form of a compound of the invention where water molecules are combined in a definite ratio as an integral part of the crystal structure of the compound.

As used herein, “solvate” is a form of of a compound of the invention where solvent molecules are combined in a definite ratio as an integral part of the crystal structure of the compound.

Depending on its structure, the phrase “pharmaceutically acceptable salt,” as used herein, refers to a pharmaceutically acceptable organic or inorganic acid or base salt of a benzamide derivative. Representative pharmaceutically acceptable salts include, e.g., alkali metal salts, alkali earth salts, ammonium salts, water-soluble and water-insoluble salts, such as the acetate, amsonate (4,4-diaminostilbene-2,2-disulfonate), benzenesulfonate, benzonate, bicarbonate, bisulfate, bitartrate, borate, bromide, butyrate, calcium, calcium edetate, camsylate, carbonate, chloride, citrate, clavulariate, dihydrochloride, edetate, edisylate, estolate, esylate, fumarate, gluceptate, gluconate, glutamate, glycollylarsanilate, hexafluorophosphate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isothionate, lactate, lactobionate, laurate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate, N-methylglucamine ammonium salt, 3-hydroxy-2-naphthoate, oleate, oxalate, palmitate, pamoate (1,1-methene-bis-2-hydroxy-3-naphthoate, einbonate), pantothenate, phosphate/diphosphate, picrate, polygalacturonate, propionate, p-toluenesulfonate, salicylate, stearate, subacetate, succinate, sulfate, sulfosaliculate, suramate, tannate, tartrate, teoclate, tosylate, triethiodide, and valerate salts. Furthermore, a pharmaceutically acceptable salt can have more than one charged atom in its structure. In this instance the pharmaceutically acceptable salt can have multiple counterions. Hence, a pharmaceutically acceptable salt can have one or more charged atoms and/or one or more counterions.

As used herein, the term “geometrical isomers” refers compounds that have the same molecular formula but the atoms are in different non-equivalent positions to one another.

As used herein, the term “optical isomers” refers to compounds with chiral atoms which have the ability to rotate plane polarized light, R/S configuration. The term optical isomer include enantiomers and diastereomers as well as compounds which can be distinguished one from the other by the designations of (D) and (L).

As used herein:

-   -   DCM means dichloromethane,     -   DEAD means diethyl azocarboxylate,     -   DMF means dimethylformamide,     -   EDCI means 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide         hydrochloride,     -   Ether means diethyl ether,     -   EtOAc means ethylacetate,     -   HOBt means 1-hydroxybenzotriazole,     -   HPLC means high-performance liquid chromatography,     -   LC means liquid chromatography,     -   MeCN means acetonitrile,     -   DPPA means diphenylphosphoryl azide,     -   RT means room temperature,     -   SM means starting material,     -   TEA means triethylamine, and     -   THF means tetrahydrofuran.

Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. The term “stable”, as used herein, refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., therapeutic administration to a subject for the treatment of disease, 11-β-HSD1 inhibition, 11-β-HSD1-mediated disease).

The term “prodrug forms” in the present description means a pharmacologically acceptable derivative, such as an ester or an amide, which derivative is biotransformed in the body to form the active drug (see Goodman and Gilman's, The Pharmacological basis of Therapeutics, 8^(th) ed., McGraw-Hill, Int. Ed. 1992, “Biotransformation of Drugs”, p. 13-15).

“Pharmaceutically acceptable” means in the present description being useful in preparing a pharmaceutical composition that is generally safe, non-toxic and neither biologically nor otherwise undesirable and includes being useful for veterinary use as well as human pharmaceutical use.

“Pharmaceutically acceptable salts” mean in the present description salts which are pharmaceutically acceptable, as defined above, and which possess the desired pharmacological activity. Such salts include acid addition salts formed with organic and inorganic acids, such as hydrogen chloride, hydrogen bromide, hydrogen iodide, sulfuric acid, phosphoric acid, acetic acid, glycolic acid, maleic acid, malonic acid, oxalic acid, methanesulfonic acid, trifluoroacetic acid, fumaric acid, succinic acid, tartaric acid, citric acid, benzoic acid, ascorbic acid and the like. Base addition salts may be formed with organic and inorganic bases, such as sodium, ammonia, potassium, calcium, ethanolamine, diethanolamine, N-methylglucamine, choline and the like. Included in the invention are pharmaceutically acceptable salts or compounds of any of the formulae herein.

Pharmaceutical compositions according to the present invention contain a pharmaceutically acceptable carrier together with at least one of the compounds of the invention as described herein above, dissolved or dispersed therein as an active, antimicrobial, ingredient. In one embodiment, the therapeutic composition is not immunogenic when administered to a human patient for therapeutic purposes, unless that purpose is to induce an immune response.

The preparation of a pharmacological composition that contains active ingredients dissolved or dispersed therein is well understood in the art. Typically such compositions are prepared as sterile injectables either as liquid solutions or suspensions, aqueous or non-aqueous, however, solid forms suitable for solution, or suspensions, in liquid prior to use can also be prepared. The preparation can also be emulsified.

The active ingredient may be mixed with excipients, which are pharmaceutically acceptable and compatible with the active ingredient and in amounts suitable for use in the therapeutic methods described herein. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol or the like and combinations thereof. In addition, if desired, the composition may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents and the like which enhance the effectiveness of the active ingredient. Adjuvants may also be present in the composition.

Pharmaceutically acceptable carriers are well known in the art. Exemplary of liquid carriers are sterile aqueous solutions that contain no materials in addition to the active ingredients and water, or contain a buffer such as sodium phosphate at physiological pH value, physiological saline or both, such as phosphate-buffered saline. Still further, aqueous carriers can contain more than one buffer salt, as well as salts such as sodium and potassium chlorides, dextrose, propylene glycol, polyethylene glycol and other solutes.

Liquid compositions can also contain liquid phases in addition to and to the exclusion of water. Exemplary of such additional liquid phases are glycerine, vegetable oils such as cottonseed oil, organic esters such as ethyl oleate, and water-oil emulsions.

The pharmaceutical composition according to one of the embodiments of the present invention comprising compounds of the invention, may include pharmaceutically acceptable salts of that component therein as set out above. Pharmaceutically acceptable salts include the acid addition salts (formed with the free amino groups of the polypeptide) that are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic acid, tartaric acid, mandelic acid and the like. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylaminoethanol, histidine, procaine and the like.

The preparations according to the embodiments may be administered orally, topically, intraperitoneally, intraarticularly, intracranially, intradermally, intramuscularly, intraocularly, intrathecally, intravenously, subcutaneously. Other routes are known to those of ordinary skill in the art.

The orally administrable compositions according to the present invention may be in the form of tablets, capsules, powders, granules, lozenges, liquid or gel preparations, such as oral, topical or sterile parenteral solutions or suspensions. Tablets and capsules for oral administration may be in unit dose presentation form and may contain conventional excipients such as binding agents, for example syrup, acacia, gelatin, sorbitol, traganath or polyvinyl-pyrrolidone; fillers e.g. lactose, sugar, maize-starch, calcium phosphate, calcium hydrogen phosphate, sodium starch glycolate, sorbitol or glycine; tabletting lubricant e.g. magnesium stearate, talc, polyethylene glycol or silicon dioxide (optionally colloidal); disintegrants e.g. potato starch, or acceptable wetting agents such as sodium lauryl sulfate. The tablets may be coated according to methods well known in normal pharmaceutical practice. Oral liquid preparations may be in the form of e.g. aqueous or oily suspensions, solutions, emulsions, syrups or elixirs or may be presented as a dry product for reconstitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, e.g. sorbitol, syrup, methyl cellulose (optionally microcrystalline), glucose syrup, gelatin hydrogenated edible fats; emulsifying agents e.g. lecithin, sorbitan monooleate or acacia, non-aqueous vehicles (which may include edible oils), e.g. almond oil, fractionated coconut oil, oily esters such as glycerine, propylene glycol, or ethyl alcohol; preservatives e.g. methyl or propyl p-hydroxybenzoate or sorbic acid, and if desired conventional flavouring or colouring agents.

“An effective amount” refers to an amount of a compound which confers a therapeutic effect on the treated subject. The therapeutic effect may be objective (i.e., measurable by some test or marker) or subjective (i.e., subject gives an indication of or feels an effect). A pharmaceutical composition according to the present invention, may comprise typically an amount of at least 0.1 weight percent of a compound of the invention per weight of total therapeutic composition. A weight percent is a ratio by weight of total composition. Thus, for example, 0.1 weight percent is 0.1 grams of a compound of the invention per 100 grams of total composition. A suitable daily oral dose for a mammal, preferably a human being, may vary widely depending on the condition of the patient. However a dose of a compound of the invention of about 0.1 to 300 mg/kg body weight may be appropriate.

The compositions according to the present invention may also be used veterinarily and thus they may comprise a veterinarily acceptable excipient or carrier. The compounds and compositions may be thus administered to animals, e.g., cats, dogs, or horses, in treatment methods.

The compounds of the present invention in labelled form, e.g. isotopically labelled, may be used as a diagnostic agent.

This invention relates to methods of making compounds of any of the formulae herein comprising reacting any one or more of the compounds of the formulae delineated herein, including any processes delineated herein. The compounds of the invention above may be prepared by, or in analogy with, conventional methods, and especially according to or in analogy with the following methods. Further, the pharmacology in-vitro was studied using the following reagents and methods.

The chemicals used in the synthetic routes delineated herein may include, for example, solvents, reagents, catalysts, and protecting group and deprotecting group reagents. The methods described above may also additionally include steps, either before or after the steps described specifically herein, to add or remove suitable protecting groups in order to ultimately allow synthesis of the compounds. In addition, various synthetic steps may be performed in an alternate sequence or order to give the desired compounds. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing applicable compounds are known in the art and include, for example, those described in R. Larock, Comprehensive Organic Transformations, VCH Publishers (1989); T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3^(rd) Ed., John Wiley and Sons (1999); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995) and subsequent editions thereof.

All publications mentioned herein are hereby incorporated by reference. By the expression “comprising” means “including but not limited to.” Thus, other non-mentioned substances, additives or carriers may be present.

The invention will now be described in reference to the following Examples. These Examples are not to be regarded as limiting the scope of the present invention, but shall only serve in an illustrative manner.

* * * EXAMPLES Biological Examples

Scintillation Proximity Assay

[1,2(n)-³H]-cortisone was purchased from Amersham Pharmacia Biotech. Anti-cortisol monoclonal mouse antibody, clone 6D6.7 was obtained from Immunotech and Scintillation proximity assay (SPA) beads coated with monoclonal antimouse antibodies were from Amersham Pharmacia Biotech. NADPH, tetrasodium salt was from Calbiochem and glucose-6-phosphate (G-6-P) was supplied by Sigma. The human 11-β-hydroxysteroid dehydrogenase type-1 enzyme (11-β-HSD₁) was expressed in Pichia pastoris. 18-β-glycyrrhetinic acid (GA) was obtained from Sigma. The serial dilutions of the compounds were performed on a Tecan Genesis RSP 150. Compounds to be tested were dissolved in DMSO (1 mM) and diluted in 50 mM Tris-HCl, pH 7.2 containing 1 mM EDTA.

The multiplication of plates was done on a WallacQuadra. The amount of the product [³H]-cortisol, bound to the beads was determined in a Packard, Top Count microplate liquid scintillation counter.

The 11-β-HSD₁ enzyme assay was carried out in 96 well microtiter plates (Packard, Optiplate) in a total well volume of 220 μL and contained 30 mM Tris-HCl, pH 7.2 with 1 mM EDTA, a substrate mixture tritiated Cortisone/NADPH (175 nM/181 μM), G-6-P (1 mM) and inhibitors in serial dilutions (9 to 0.15 μM). Reactions were initiated by the addition of human 11-β-HSD1, either as Pichia pastoris cell homogenate or microsomes prepared from Pichia pastoris (the final amount of enzyme used was varied between 0.057 to 0.11 mg/mL). Following mixing, the plates were shaken for 30 to 45 minutes at room temperature. The reactions were terminated with 10 μL 1 mM GA stop solution. Monoclonal mouse antibody was then added (10 μL of 4 μM) followed by 100 μL of SPA beads (suspended according to the manufacturers instructions). Appropriate controls were set up by omitting the 11-β-HSD, to obtain the non-specific binding (NSB) value.

The plates were covered with plastic film and incubated on a shaker for 30 minutes, at room temperature, before counting. The amount of [³H]-cortisol, bound to the beads was determined in a microplate liquid scintillation counter. The calculation of the K_(i) values for the inhibitors was performed by use of Activity Base. The K_(i) value is calculated from IC₅₀ and the K_(m) value is calculated using the Cheng Prushoff equation (with reversible inhibition that follows the Michaelis-Menten equation): K_(i)=IC₅₀(1+[S]/K_(m)) [Cheng, Y. C.; Prushoff, W. H. Biochem. Pharmacol. 1973, 22, 3099-3108]. The IC₅₀ is measured experimentally in an assay wherein the decrease of the turnover of cortisone to cortisol is dependent on the inhibition potential of each substance. The Ki values of the compounds of the present invention for the 11-β-HSD1 enzyme lie typically between about 10 nM and about 10 μM. Below follow some Ki examples according to the present invention.

Example Ki value (nM) 10 250 14 107 48 174 Cloning, Expression and Purification of 11β-HSD1

The expression and purification of the murine enzyme is described by J. Zhang, et al. Biochemistry, 44, 2005, pp 6948-57. The expression and purification of the human enzyme is similar to that of the murine sequence.

Enzyme Assay:

The IC50 and Ki of the compounds are determined by the following method:

-   -   1. Prepare an Assay Buffer, (pH 7.2, 50 mM Tris-HCL, 1 mM EDTA)         fresh each week.     -   2. Prepare the following solutions:         -   NADPH (Sigma, 200 μM)         -   ³H-Cortisone (Amersham Biosciences, 45 Ci/mmol, 200 nM)         -   Enzyme Prep (20 nM for human, 10 nM for mouse)         -   Cortisol Antibody (East Coast Biologicals, (1:50 dilution)         -   Anti-mouse SPA beads (Amersham Biosciences, 15 mg/ml)         -   18β-Glycyrrhetinic acid (“GA”) (Aldrich, 1 μM)         -   Compound Stock Solution (10 mM in DMSO), serially diluted in             assay buffer. Each compound is tested at six different             concentrations usually (10 μM to 0.1 nM). All of the             solutions and dilutions are made in the Assay Buffer.     -   3. Assay is run using white/white, 96-well assay plates         (Corning) in a total volume of 100 μL.     -   4. Into each well of a 96-well plate is added Assay Buffer (30         μL), compound (10 μL ) NADPH (10 μL), and ³H-cortisone (10 μL).     -   5. Initiate reaction by adding 40 μL of HSD-1 enzyme prep to the         wells.     -   6. The plate is covered with tape and incubated on an orbital         shaker for 1 h at RT.     -   7. After 1 h, the tape is removed and anti-cortisol antibody (10         μL), GA solution (10 μL), and SPA bead preparation (100 μL) is         added.     -   8. The plate is incubated (30 min) on an orbital shaker at RT.     -   9. The counts are read on a TopCount NXT reader.     -   10. A dose-response curve is first plotted using the Graphpad         Prism software, to generate the IC50 values.

With this IC50 value and the known Km value for the substrate and HSD1 enzyme, an estimated Ki can be calculated with the Chen and Prusoff equation {Ki=IC50/[1+(substrate/Km)]}.

In addition to the above examples, the compounds of the present invention all show 11β-HSD1 enzyme activity (IC₅₀) in the assays ranging from 10 nM and 10 μM.

The following compounds exhibited activity in the Enzyme assay with IC₅₀ values less than 20 nM:

-   2-((3-chloro-2-methylphenyl)amino)-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   5-methyl-5-(pyridin-4-yl)-2-(2-(trifluoromethyl)phenylamino)thiazol-4(5H)-one; -   2-((2-chlorophenyl)amino)-5-methyl-5-phenyl-1,3-thiazol-4(5H)-one; -   (5S)-2-((2-chlorophenyl)amino)-5-methyl-5-phenyl-1,3-thiazol-4(5H)-one; -   (5R)-2-((2-chlorophenyl)amino)-5-methyl-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   2-((2-chlorophenyl)amino)-5-methyl-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   2-((S)-1-cyclohexylethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one; -   (5S,7R)-2-(cyclooctylamino)-7-(methyloxy)-1-thia-3-azaspiro[4.5]dec-2-en-4-one; -   2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-((tetrahydro-2H-pyran-4-yl)methyl)thiazol-4(5H)-one; -   2-((5-fluoro-2-methylphenyl)amino)-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   2-(2-chlorophenylamino)-5-methyl-5-(tetrahydro-2H-pyran-4-yl)thiazol-4(5H)-one; -   2-((R)-1-(4-fluorophenyl)ethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one; -   2-((2,5-difluorophenyl)amino)-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   2-(cyclohexylmethylamino)-5-methyl-5-((S)-tetrahydrofuran-3-yl)thiazol-4(5H)-one; -   5-methyl-5-(1-methylethyl)-2-((2-(trifluoromethyl)phenyl)amino)-1,3-thiazol-4(5H)-one; -   2-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-propylthiazol-4(5H)-one; -   2-(o-toluidino)-5-cyclopentylthiazol-4(5H)-one; -   2-((2-fluorophenyl)amino)-1-thia-3-azaspiro[4.4]non-2-en-4-one; -   2-((3-fluorotricyclo[3.3.1.1˜3,7˜]dec-1-yl)amino)-5-methyl-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   (R)-5-isopropyl-5-methyl-2-((S)-1-phenylethylamino)thiazol-4(5H)-one; -   2-((2,6-dichlorophenyl)amino)-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   2-(cyclohexylmethylamino)-5-((S)-tetrahydrofuran-3-yl)thiazol-4(5H)-one; -   2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-1,3-thiazol-4(5H)-one; -   2-(2-chlorophenylamino)-5-cyclopentylthiazol-4(5H)-one; -   2-(2-chlorophenylamino)-5-cyclohexylthiazol-4(5H)-one; -   2-((2-chlorophenyl)amino)-5-(1-methylethyl)-1,3-thiazol-4(5H)-one; -   2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-5-(pyridin-4-yl)thiazol-4(5H)-one; -   2-((S)-1-(2-fluorophenyl)ethylamino)-5-methyl-5-(pyridin-4-yl)thiazol-4(5H)-one; -   2-(2-fluorophenylamino)-5-((S)-tetrahydrofuran-3-yl)thiazol-4(5H)-one; -   2-((1R,2R,4S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(2,2,2-trifluoroethyl)thiazol-4(5H)-one; -   5-ethyl-5-methyl-2-(tricyclo[3.3.1.1˜3,7˜]dec-1-ylamino)-1,3-thiazol-4(5H)-one; -   2-(2-chlorophenylamino)-5-methyl-5-(pyridin-4-yl)thiazol-4(5H)-one; -   5-cyclopentyl-2-(2-fluorophenylamino)thiazol-4(5H)-one; -   5-cyclohexyl-2-(2-fluorophenylamino)thiazol-4(5H)-one; -   2-((R)-1-(2-fluorophenyl)ethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one; -   (R)-2-((S)-1-(2-fluorophenyl)ethylamino)-5-isopropyl-5-methylthiazol-4(5H)-one;     and     2-((2,4-dichlorophenyl)amino)-5-(1-methylethyl)-1,3-thiazol-4(5H)-one.

Synthesis Examples

General Reaction Schemes

All commercial starting materials are used without any purification.

If the appropriate α-bromocarboxylic acid or ester not is commercially available, the substances has been prepared in accordance to this method:

The 2-amino-carboxylic acid (1.0 eq.) was suspended in 2.0 M H₂SO₄ (4 eq.), KBr (8 eq.) was added and the mixture was cooled in an ice-bath. NaNO₂ (1.3 eq.) dissolved in water was added slowly. The reaction mixture was stirred for 4 h at ice-bath, before allowed to reach room temperature. The reaction mixture was extracted with EtOAc. The organic phase was dried over MgSO₄ before concentrated in vacuum. This gave the crude product which was used in the next step without further purification (J. Org. Chem. 2002, 67 (11), 3595-3600; Xinhua Qian; Bin Zheng; Brian Burke; Manohar T. Saindane and David R. Kronenthal).

Methods and Materials

¹H nuclear magnetic resonance (NMR) and ¹³C NMR were recorded on a Bruker PMR 500 spectrometer at 500.1 MHz and 125.1 MHz, respectively or on a JEOL eclipse 270 spectrometer at 270.0 MHz and 67.5 MHz, respectively. All spectra were recorded using residual solvent or tetramethylsilane (TMS) as internal standard. IR spectra were recorded on a Perkin-Elmer Spectrum 1000 FT-IR spectrometer. Electrospray mass spectrometry (MS) was obtained using an Agilent MSD mass spectrometer. Accurate mass measurements were performed on a Micromass LCT dual probe. Elemental analyses were performed on a Vario E1 instrument or sent to Mikro Kemi in Uppsala.

Analytical HPLC were performed on Agilent 1100 system equipped with System A: ACE 3 (C8, 50×3.0 mm) or System B: YMC ODS-AQ, (33×3.0 mm) using the eluent system: water/0.1% TFA and CH₃CN, 1 mL/min, with a gradient time of 3 min.

Preparative HPLC was performed on a Gilson system equipped with System A: ACE 5 C8 column (50×20 mm) gradient time 5 min, system B: YMC ODS-AQ (150×30 mm) gradient time 8.5 min or system C: YMC ODS-AQ (50×20 mm) gradient time 5 min using the eluent system: water/0.1% TFA and CH₃CN. Preparative flash chromatography was performed on Merck silica gel 60 (230-400 mesh).

Synthetic Methodology

Method A or B was used depending on whether the isothiocyanate or the corresponding amine was used. The amine or the isothiocyanate was purchased from either Maybridge Plc. or from Sigma-Aldrich Co.

Method A

1.0 eq. of the appropriate isothiocyanate was stirred in 2 M ammonia in ethanol (5 eq.) for 18 h at RT. Evaporation in vacuo afforded the crude product, which crystallized upon addition of DCM. The crystals were collected on a filter and air-dried to afford the thiourea.

Method B

1.0 eq. of the amine and ethoxycarbonylisothiocyanate (1.0 eq) were mixed in a test tube. A violently exothermic reaction resulted in a white paste. This was taken up in 5M KOH solution and stirred at 70° C. for 2 hours at which point LC analysis indicated full hydrolysis of the intermediate. The mixture was cooled, diluted with water and extracted 3 times with chloroform. Subsequent preparative LC yielded the desired thiourea.

Method C

The thiourea (1.0 eq.) and the α-bromoester/(α-bromoacid (1.0 eq.) was dissolved in acetone and heated to 60° C. in a sealed tube for 15-72 hours. The solvent was removed. And the product purified by crystallization from MeOH/preparative reverse-phase HPLC.

Method C1

The thiourea (1.0 eq.) and the α-bromoester/α-bromoacid (1.0 eq.) was mixed in water and heated in the microwave at 140° C. for 1 hour. The aqueous phase was extracted twice with DCM. The combined organic phases were evaporated and the obtained crude product was purified by preparative reverse-phase HPLC.

Method D

The thiourea (1.0 eq.) and the α-bromoester (1.0 eq.) was dissolved in 1,4-dioxane and heated to 100° C. in a sealed tube for 1-11 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.

Method D1

The thiourea (1.0 eq.) and the α-bromoester (1.0 eq.) was dissolved in THF and heated to 70° C. in a sealed tube for 1 day. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.

Method D2

The thiourea (1.0 eq.) and the α-bromoester (1.0 eq.) was dissolved in 2-propanol and heated to 95° C. in a sealed tube for 3 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.

Method D3

The thiourea (1.0 eq.) and the α-bromoester/α-bromoacid (1.0 eq.) was dissolved in MeCN and heated to 60° C. in a sealed tube for 2 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC.

Method E

The amino acid (1 eq.) was suspended in 2.0 M H₂SO₄, KBr (8 eq.) was added and the mixture was cooled in an ice-bath. NaNO₂ (1.3 eq.) dissolved in water was slowly added. The reaction mixture was stirred for 4 h while cooling was continued. The reaction mixture was then extracted with EtOAc, washed with brine and brine containing Na₂S₂O₃. The organic phase was concentrated in vacuum. The product was used in the next step without further purification.

Method F

The thiourea (1 eq.) and 3-bromo-2-coumarone (1 eq.) was dissolved in acetone and heated to 60° C. for 3 hours. Water was added. The obtained solid was collected. Recrystallised from water/MeCN. The solid was collected. The mother liquor was concentrated and the obtained solid was dried in vacuum to give the product.

Method G

The carbonate salt of guanidine (1 eq.) and the alpha hydroxy ester (1 eq.) was dissolved in EtOH and heated to reflux for 2-10 hours. The mixture was then poured in to H₂O and left at 8° C. for 16 hours. The product was collected by filtration.

Method H

The amino-oxazolone (1 eq.) and the amine (3 eq.) was added to 4 ml EtOH and put in the microwave oven at 130° C. for 30 min. The solvent was removed under vacuum and the products purified by preparative reverse-phase HPLC.

Method I

To an ice-cooled solution with 1 eq. of the thiourea in DCM was 3 eq. 5% NaOH (aq) and 2 eq. dibromobutyryl chloride added followed by a small amount of benzyltriethylammonium chloride. The reaction was allowed to reach rt and additional 5 eq. 5% NaOH (aq) was added. The DCM-layer was separated and washed twice with water, dried over MgSO₄, filtered and concentrated. The product was isolated by preparative reverse-phase HPLC.

Method J

The acid (1 eq.) was dissolved in SOCl₂ and heated to 60° C. for 2 hours. NBS (2 eq.), SOCl₂ and 1 drop of HBr (aq) was added at r.t. The reaction was heated to reflux for 75 min. The solvent was removed under vacuum, CCl₄ was added and this was filtered. CCl₄ was removed under vacuum. The remaining oil was dissolved in EtOH and left for 16 hours at r.t. The solvent was then removed under vacuum. This gave the product as an α-bromoester.

EXAMPLES

Methods A-J were employed for preparing the compounds of Examples 1-79 as described below.

Example 1 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and ethyl 2-bromoisovalerate according to Method C.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.79 (m, 3 H), 0.97 (m, 3 H), 1.10 (m, 3 H), 1.45 (m, 4 H), 1.69 (m, 1 H), 2.22 (m, 2 H), 2.36 (m, 1 H), 3.74 (m, 1 H), 4.37 (m, 1 H), 9.56 (s, 1 H). MS (ESI+) for C₁₃H₂₀N₂OS m/z 253 (M+H)⁺.

Example 2 2-(bicyclo[2.2.1]hept-2-ylamino)-5-ethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and ethyl 2-bromobutyrate according to Method C.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.90 (m, 3 H), 1.03-1.23 (m, 3 H), 1.35-1.56 (m, 4 H), 1.65-1.84 (m, 2 H), 1.98 (m, 1 H), 2.24 (m, 2 H), 3.75 (m, 1 H), 4.22-4.40 (m, 1 H), 9.84 (s, 1 H). MS (ESI+) for C₁₂H₁₈N₂OS m/z 239 (M+H)⁺.

Example 3 2-(bicyclo[2.2.1]hept-2-ylamino)-5-phenyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and methyl alpha-bromophenylacetate according to Method C.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 1.05-1.24 (m, 3 H), 1.36-1.56 (m, 4 H), 1.66-1.80 (m, 1 H), 2.22-2.33 (m, 2 H), 3.78-3.90 (m, 1 H), 5.41 (s, 0.5 H), 5.43 (s, 0.5 H), 7.21-7.41 (m, 5 H), 9.39 (d, J=6.35 Hz, 1 H). MS (ESI+) for C₁₆H₁₈N₂OS m/z 287 (M+H)⁺.

Example 4 2-(cyclohexylamino)-5-ethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from n-cyclohexylthiourea and ethyl 2-bromobutyrate according to Method C. Gave 201 mg (75%).

¹H NMR (400 ^(MHz), DMSO-d₆) δ ppm 0.91 (m, 3 H), 1.05-2.06 (m, 12 H), 3.76 (m, 1 H), 4.36 (m, 1 H), 10.11 (s, 1 H). MS (ESI+) for C₁₁H₁₈N₂OS m/z 227 (M+H)⁺

Example 5 2-(bicyclo[2.2.1]hept-2-ylamino)-5,5-dimethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and Ethyl 2-bromoisobutyrate according to Method C.

¹H NMR (400 ^(MHz), DMSO-d₆) δ ppm 1.05-1.21 (m, 3 H), 1.34-1.54 (m, 4 H), 1.48 (s, 2 H), 1.49 (s, 2 H), 1.50 (s, 1 H), 1.51 (s, 1 H), 1.67-1.74 (m, 1 H), 2.18-2.28 (m, 2 H), 3.20 (dd, J=7.69, 2.93 Hz, 0.25 H), 3.73-3.82 (m, 0.75 H), 9.12 (d, J=6.59 Hz, 1 H). MS (ESI+) for C₁₂H₁₈N₂OS m/z 239 (M+H)⁺

Example 6 5-Isopropyl-2-(tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-1,3-thiazol-4(5H)-one

Synthesis was performed from N-tricyclo[3.3.1.0˜3,7˜]non-3-ylthiourea and ethyl 2-bromo-3-methylbutanoate according to Method C.

¹H NMR (400 MHz, DMSO-d₆) δ 0.75 (d, J=6.6 Hz, 3 H), 0.95 (d, J=6.8 Hz, 3 H), 1.46-1.57 (m, 4 H), 1.88-2.10 (m, 6 H), 2.22-2.37 (m, 3 H), 2.43 (t, J=6.7 Hz, 1 H), 4.23 (d, J=3.5 Hz, 1 H), 9.29 (s, 1 H). MS (ESI+) for C₁₅H₂₂N₂OS m/z 279 (M+H)^(+.)

Example 7 6-(tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-tricyclo[3.3.1.0˜3,7˜]non-3-ylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D.

¹H NMR (400 ^(MHz), DMSO-d₆) δ 1.45-1.57 (m, 4 H), 1.90-2.16 (m, 8 H), 2.22-2.27 (m, 2 H), 2.44-2.55 (m, 5 H, obscured by solvent signal), 9.24 (s, 1 H). MS (ESI+) for C₁₅H₂₀N₂OS m/z 277 (M+H)^(+.)

Example 8 2-(Tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-1,3-thiazol-4(5H)-one

Synthesis was performed from N-tricyclo[3.3.1.0˜3,7˜]non-3-ylthiourea and ethyl bromoacetate according to Method D1.

¹H NMR (400 MHz, DMSO-d₆) δ 1.45-1.61 (m, 4 H), 1.92-2.07 (m, 6 H), 2.23 (m, 1.7 H, major rotamer), 2.82 (m, 0.3 H, minor rotamer), 2.45 (t, J=6.7 Hz, 0.85 H, major rotamer), 2.66 (t, J=6.8 Hz, 0.15 H, minor rotamer), 3.83 (s, 1.7 H, major rotamer), 4.09 (s, 0.3 H, minor rotamer), 9.38 (s, 1 H). MS (ESI+) for C₁₂H₁₆N₂OS m/z 237 (M+H)⁺.

Example 9 6-(Cyclooctylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-cyclooctylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D2.

¹H NMR (400 MHz, DMSO-d₆) δ 1.45-1.79 (m, 14 H), 1.86-2.00 (m, 1 H), 2.05-2.17 (m, 1 H), 2.41-2.53 (m, 4 H, obscured by solvent signal), 4.01 (m, 1 H), 9.09 (d, J=7.5 Hz, 1 H).

¹³C NMR (100 MHz, DMSO-d₆) δ 16.31, 23.07, 24.97, 26.69, 30.88, 33.52, 54.69, 60.30, 175.09, 191.25. MS (ESI+) for C₁₄H₂₂N₂OS m/z 267 (M+H)⁺.

Example 10 6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-cycloheptylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D.

¹H NMR (⁴⁰⁰ MHz, DMSO-d₆) δ 1.35-1.65 (m, 10 H), 1.83-1.97 (m, 3 H), 2.05-2.17 (m, 1 H), 2.41-2.53 (m, 4 H, obscured by solvent signal), 3.96 (m, 1 H), 9.09 (d, J=7.5 Hz, 1 H). MS (ESI+) for C₁₃H₂₀N₂OS m/z 253 (M+H)^(+.)

Example 11 6-(Bicyclo[2.2.1]hept-2-ylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D.

¹H NMR (⁴⁰⁰ MHz, DMSO-d₆) δ 1.05-1.22 (m, 3 H), 1.33-1.49 (m, 4 H), 1.63-1.70 (m, 1 H), 1.86-2.00 (m, 1 H), 2.05-2.22 (m, 3 H), 2.42-2.53 (m, 4 H, obscured by solvent signal), 3.74 (m, 1 H), 8.98 (d, J=7.5 Hz, 1 H). MS (ESI+) for C₁₃H₁₈N₂OS m/z 251 (M+H)⁺.

Example 12 6-[(2,2,3,3-Tetramethylcyclopropyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-(2,2,3,3-tetramethylcyclopropyl)thiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D.

¹H NMR (400 MHz, DMSO-d₆) δ 0.92 (s, 3 H), 0.94 (s, 3 H), 1.06 (s, 3 H), 1.08 (s, 3 H), 1.88-2.00 (m, 1 H), 2.01 (s, 1 H), 2.06-2.17 (m, 1 H), 2.40-2.54 (m, 4 H, obscured by solvent signal), 8.78 (s br., 1 H). MS (ESI+) for C₁₃H₂₀N₂OS m/z 253 (M+H)^(+.)

Example 13 6-[(2-Methylphenyl)amino]-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-(2-methylphenyl)thiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D.

¹H NMR (⁴⁰⁰ MHz, DMSO-d₆) δ 1.89 (m, 1 H), 2.04-2.13 (m, 1 H), 2.08 (s, 3 H), 2.39-2.48 (m, 2 H), 2.56-2.66 (m, 2 H), 6.81 (d, J=7.6 Hz, 1 H), 7.03 (m, 1 H), 7.14 (m, 1 H), 7.20 (d, J=7.4 Hz, 1 H), 11.67 (s br., 1 H). MS (ESI+) for C₁₃H₁₄N₂OS m/z 247 (M+H)^(+.)

Example 14 2-[(cyclohexylmethyl)amino]-5,5-dimethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(cyclohexylmethyl)thiourea and ethyl 2-bromoisobutyrate according to Method C.

¹H NMR (270 MHz, DMSO-d₆) δ ppm 0.81-1.04 (m, 2 H), 1.03-1.32 (m, 3 H), 1.43-1.54 (m, 6 H), 1.55-1.78 (m, 6 H), 3.18-3.32 (m, 2 H), 9.28 (s, 1 H). MS (ESI+) for C₁₂H₂₀N₂OS m/z 242 (M+H)^(+.)

Example 15 2-[(2-fluorophenyl)amino]-5-isopropyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-fluorophenyl)thiourea and Ethyl 2-bromo-2-methylbutyrate according to Method C.

¹H NMR (²⁷⁰ MHz, DMSO-d₆) δ ppm 0.79-0.98 (m, 6 H), 2.29-2.44 (m, 1 H), 4.48 (d, J=3.59 Hz, 1 H), 6.91-7.40 (m, 4 H). MS (ESI+) for C₁₂H₁₃FN₂OS m/z 253 (M+H)^(+.)

Example 16 2-[(cyclohexylmethyl)amino]-5-(2-hydroxyphenyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(cyclohexylmethyl)thiourea and 3-bromo-2-coumarone according to Method F.

¹H NMR (⁴⁰⁰ MHz, CHLOROFORM-D) δ ppm 0.80-1.00 (m, 2H), 1.05-1.27 (m, 3H), 1.55-1.81 (m, 6H), 3.24-3.34 (m, 2H), 5.42 (s, 1H), 6.73-6.81 (m, 2H), 7.02-7.14 (m, 2H), 9.19 (br.s, 1H, N—H), 9.81 (br.s, 1H, N—H). MS (ESI+) for C₁₆H₂₀N₂O₂S m/z 305 (M+H)⁺.

Example 17 (5S)-2-(cycloheptylamino)-5-methyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-cycloheptylthiourea and (2S)-2-bromopropanoic acid according to Method C.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.35-1.70 (m, 12H), 1.45 (d, J=7.3 Hz, 3H), 1.72-2.00 (m, 1H), 3.90-4.03 (m, 1H). MS (ESI+) for C₁₁H₁₈N₂OS m/z 227 (M+H)^(+.)

Example 18 (5R)-2-(cycloheptylamino)-5-methyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-cycloheptylthiourea and (2R)-2-bromopropanoic acid according to Method C.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.36-1.70 (m, 12H), 1.45 (d, J=7.5 Hz, 3H), 1.82-1.96 (m, 1H), 3.93-4.02 (m, 1H). MS (ESI+) for C₁₁H₁₈N₂OS m/z 227 (M+H)^(+.)

Example 19 2-(cycloheptylamnino)-5-ethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-cycloheptylthiourea and 2-bromobutyric acid according to Method C.

¹H NMR (270 MHz, METHANOL-d₄) δ ppm 0.90-1.06 (m, 3 H), 1.40-2.17 (m, 14 H), 4.26 (dd, J=7.86, 4.02 Hz, 1 H), 4.52-4.68 (m, 1 H). MS (ESI+) for C₁₂H₂₀N₂OS m/z 241 (M+H)^(+.)

Example 20 2-(cycloheptylamino)-5-isopropyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-cycloheptylthiourea and Ethyl 2-bromo-2-methylbutyrate according to Method C.

¹H NMR (270 MHz, METHANOL-d₄) mixture of three different rotamers ˜40%/30%/30% only the major; δ ppm 0.92-1.08 (m, 6 H), 1.43-2.16 (m, 12 H), 2.39-2.56 (m, 1 H), 3.98-4.20 (m, 1 H), 4.24-4.34 (m, 1 H). MS (ESI+) for C₁₃H₂₂N₂OS m/z 255 (M+H)^(+.)

Example 21 5-tert-butyl-2-(cycloheptylamino)-1,3-thiazol-4(5H)-one

Synthesis was performed from 2-amino-3,3-dimethylbutanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, METHANOL-d₄) δ ppm 0.83-0.94 (m, 4.5 H), 0.98-1.12 (m, 4.5 H), 1.47-1.97 (m, 11 H), 2.36-2.58 (m, 1 H), 4.03-4.18 (m, 1 H), 4.34-4.42 (m, 1 H). MS (ESI+) for C₁₄H₂₄N₂OS m/z 269 (M+H)^(+.)

Example 22 2-(cyclooctylamino)-5-ethyl-1,3-thiazol-4(5B)-one

Synthesis was performed from N-cyclooctyl-thiourea and 2-bromo-butyric acid according to Method C1.

¹H NMR (270 MHz, ^(METHANOL)-d₄) δ ppm 0.89-1.03 (m, 3 H), 1.43-1.99 (m, 15 H), 1.98-2.16 (m, 1 H), 4.21-4.32 (m, 1 H), 4.55-4.66 (m, 1 H). MS (ESI+) for C₁₃H₂₂N₂OS m/z 255 (M+H)^(+.)

Example 23 5-isopropyl-2-[(2-isopropylphenyl)amino]-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-isopropylphenyl)thiourea and 2-bromo-3-methylbutyric acid according to Method C1.

¹H NMR (270 MHz, DMSO-d₆) δ ppm 0.87 (dd, J=8.78, 6.80 Hz, 6 H), 1.12-1.17 (m, 6 H), 2.28-2.44 (m, 1 H), 2.93-3.09 (m, 1 H), 4.40 (d, J=3.46 Hz, 1 H), 6.83 (dd, J=7.24, 1.79 Hz, 1 H), 7.07-7.21 (m, 2 H), 7.26-7.36 (m, 1 H).

MS (ESI+) for C₁₅H₂₀N₂OS m/z 277 (M+H)^(+.)

Example 24 5-ethyl-2-[(2-isopropylphenyl)amino]-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-isopropylphenyl)thiourea and 2-bromo-butyric acid according to Method C1.

¹H NMR (270 MHz, DMSO-d₆) δ ppm 0.88 (t, J=7.30 Hz, 3 H), 1.14 (d, J=6.93 Hz, 6 H), 1.63-2.06 (m, 2 H), 2.93-3.11 (m, 1 H), 4.32 (dd, J=7.36, 4.27 Hz, 1 H), 6.75-6.92 (m, 1 H), 7.06-7.21 (m, 2 H), 7.24-7.42 (m, 1 H). MS (ESI+) for C₁₄H₁₈N₂OS m/z 263 (M+H)⁺.

Example 25 2-[(2-chlorophenyl)amino]-5-ethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-chlorophenyl)thiourea and 2-bromo-butyric acid according to Method C1.

¹H NMR (270 MHz, METHANOL-d₄) δ ppm 1.01-1.23 (m, 3 H), 1.98-2.34 (m, 2 H), 4.58-4.72 (m, 1 H), 7.28-7.54 (m, 3 H), 7.54-7.68 (m, 1 H). MS (ESI+) for C₁₁H₁₁ClN₂OS m/z 255 (M+H)^(+.)

Example 26 5-ethyl-2-[(2-methylphenyl)amino]-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-methylphenyl)thiourea and 2-bromo-butyric acid according to Method C1.

¹H NMR (270 ^(MHz), METHANOL-d₄) δ ppm 1.07-1.18 (m, J=7.36, 7.36 Hz, 3 H), 1.98-2.36 (m, 2 H), 2.11-2.13 (m, 3 H), 4.52-4.75 (m, 1 H), 7.12 (dd, J=20.54, 7.67 Hz, 1 H), 7.22-7.46 (m, 3 H). MS (ESI+) for C₁₂H₁₄N₂OS m/z 235 (M+H)^(+.)

Example 27 5-isopropyl-2-[(2,2,3,3-tetramethylcyclopropyl)amino]-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2,2,3,3-tetramethylcyclopropyl)thiourea and ethyl-2-bromoisovalerate according to Method C.

¹H NMR (400 MHz, CDCl₃) δ ppm 0.99 (d, J=6.6 Hz, 3 H), 1.08-1.16 (m, 9 H), 1.20 (d, J=3.4 Hz, 6 H), 2.17 (s, 1 H), 2.59-2.72 (m, 1 H), 4.25 (d, J=3.9 Hz, 1 H). MS (ES+) m/z 255 (M+H⁺).

Example 28 2-(bicyclo[2.2.1]hept-2-ylamino)-5-(4-hydroxybenzyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid and N-bicyclo[2.2.1]hept-2-ylthiourea according to Method E and C.

¹H NMR (270 MHz, DMSO-d₆) δ 1.11 (d, J=9.65 Hz, 3 H), 1.24-1.54 (m, 4 H), 1.56-1.76 (m, 1 H), 2.04-2.27 (m, 2 H), 2.61-2.84 (m, 1 H), 3.26 (dd, J=14.10, 3.96 Hz, 1 H), 3.70 (s, 1 H), 4.42-4.52 (obscured by HDO peak) (m, 1 H), 6.57-6.72 (m, 2 H), 6.92-7.08 (m, 2 H), 9.07 (d, J=6.19 Hz, 1 H).

¹H NMR (270 MHz, METHANOL-d₄) δ 1.07-1.62 (m, 7 H), 1.67-1.88 (m, 1 H), 2.07-2.36 (m, 2 H), 2.92-3.11 (m, 1 H), 3.32-3.44 (partly obscured by MeOD peak) (m, 1 H), 3.64-3.76 (m, 1 H), 4.51-4.68 (m, 1 H), 6.62-6.76 (m, 2 H), 6.99-7.12 (m, 2 H). MS (ESI+) for C₁₇H₂₀N₂O₂S m/z 317 (M+H)⁺

Example 29 5-[(cyclohexylmethyl)amino]-4-thia-6-azaspiro[2.4]hept-5-en-7-one

Synthesis was performed from N-(cyclohexylmethyl)thiourea according to Method I.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.94-1.07 (m, 2 H), 1.10-1.36 (m, 3 H), 1.49-1.54 (m, 2 H), 1.66-1.86 (m, 8 H), 3.19 (d, J=6.59 Hz, 2 H). MSm/z 239 (M+H)⁺

Example 30 2-(cycloheptylamino)-5-(3,4-dihydroxybenzyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (500 MHz, Solvent) δ 1.43-1.57 (m, 6 H), 1.56-1.73 (m, 5 H), 1.84-2.01 (m, 2 H), 2.87 (dd, J=14.13, 9.42 Hz, 1 H), (1H hidden in MeOD peak) 3.97-4.06 (m, 1 H), 4.44-4.51 (m, 1 H), 6.52-6.57 (m, 1 H), 6.64-6.68 (m, 2 H). MS (ESI+) for C₁₇H₂₂N₂O₃S m/z 335 (M+H)⁺

Example 31 2-(cycloheptylamino)-5-(1H-imidazol-4-ylmethyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-(1H-imidazol-4-yl)propanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (²⁷⁰ MHz, METHANOL-d₄) δ 1.43-2.06 (m, 12 H), 3.33-3.56 (m, 2 H), 3.93-4.08 (m, 1 H), 4.57-4.69 (m, 1 H), 7.27-7.42 (m, 1 H), 8.76-8.87 (m, 1 H). MS (ESI+) for C₁₄H₂₀N₄OS m/z 293 (M+H)⁺

Example 32 2-(cycloheptylamnino)-5-isobutyl-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-4-methylpentanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, METHANOL-d₄) δ 0.91-1.04 (m, 6 H), 1.43-1.86 (m, 12 H), 1.92-2.12 (m, 3 H), 3.95-4.11 (m, 1 H), 4.29-4.48 (m, 1 H). MS (ESI+) for C₁₄H₂₄N₂OS m/z 269 (M+H)⁺

Example 33 2-(cycloheptylamino)-5-(1H-indol-3-ylmethyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, CHLOROFORM-D) δ 1.27-1.80 (m, 11 H), 1.84-1.99 (m, 1 H), 3.23-3.40 (m, 2 H), 3.76 (dd, J=15.09, 3.46 Hz, 1 H), 4.65 (d, J=9.15, 3.96 Hz, 1 H), 7.10-7.28 (m, 3 H), 7.40 (d, J=7.92 Hz, 1 H), 7.59 (d, J=7.92 Hz, 1 H), 8.26 (s, 1 H). MS (ESI+) for C₁₉H₂₃N₃OS m/z 342 (M+H)⁺

Example 34 2-(cycloheptylamino)-5-(4-hydroxybenzyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-(4-hydroxyphenyl)propanoicacid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, METHANOL-d₄) δ ppm 1.37-2.07 (m, 12 H), 2.91-3.11 (m, 1 H), 3.32-3.43 (m, 1 H), 3.86-4.02 (m, 1 H), 4.48-4.66 (m, 1 H), 6.60-6.76 (m, 2 H), 6.99-7.11 (m, 2 H). MS (ESI+) for C₁₇H₂₂N₂O₂S m/z 319 (M+H)⁺

Example 35 (5R)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-cyclohexylpropanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, CHLOROFORM-D) δ ppm 0.85-1.90 (m, 22 H), 1.93-2.10 (m, 2 H), 2.14-2.30 (m, 1 H), 3.35-3.57 (m, 1 H), 4.23 (dd, J=11.32, 3.77 Hz, 1 H). MS (ESI+) for C₁₇H₂₈N₂OS m/z 309 (M+H)⁺

Example 36 2-(cyclooctylamino)-5-(4-hydroxybenzyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid and N-cyclooctylthiourea according to Method E and C.

¹H NMR (270 MHz, CHLOROFORM-D) δ ppm 1.41-1.95 (m, 14 H), 3.07 (dd, J=14.47, 9.65 Hz, 1 H), 3.43-3.59 (m, 2 H), 4.46 (dd, J=9.65, 3.96 Hz, 1 H), 6.81 (d, J=8.41 Hz, 2 H), 7.08 (d, J=8.41 Hz, 2 H). MS (ESI+) for C₁₈H₂₄N₂O₂S m/z 333 (M+H)⁺

Example 37 (5S)-2-(cycloheptylamino)-5-(cyclohexylmethyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2R)-2-amino-3-cyclohexylpropanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, CHLOROFORM-D) δ ppm 0.87-1.86 (m, 22 H), 1.89-2.11 (m, 2 H), 2.11-2.30 (m, 1 H), 3.34-3.60 (m, 1 H), 4.23 (dd, J=11.32, 3.77 Hz, 1 H), 8.81 (br.s, 1 H). MS (ESI+) for C₁₇H₂₈N₂OS m/z 309 (M+H)⁺

Example 38 [2-(cycloheptylamino)-4-oxo-4,5-dihydro-1,3-thiazol-5-yl]acetonitrile

Synthesis was performed from (2S)-2-amino-3-cyanopropanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, ^(CHLOROFORM)-D) δ ppm 1.36-2.14 (m, 12 H), 2.85-3.11 (m, 1 H), 3.12-3.32 (m, 1 H), 3.43-3.58 (m, 1 H), 4.31-4.46 (m, 1 H). MS (ESI+) for C₁₂H₁₇N₃OS m/z 252 (M+H)⁺

Example 39 5-ethyl-2-[(3-methylphenyl)amino]-1,3-thiazol-4(5H)-one

Commercial compound, SPECS.

MS (ESI+) for C₁₂H₁₄N₂OS m/z 235 (M+H)⁺

HPLC 99%, R_(T)=2.10 min (System A, 10-97% MeCN over 3 min).

HPLC 99%, R_(T)=1.58 min (System B, 10-97% MeCN over 3 min).

Example 40 2-(cycloheptylamino)-5-(pyridin-3-ylmethyl)-1,3-thiazol-4(5H)-one

Synthesis was performed from (2S)-2-amino-3-pyridin-3-ylpropanoic acid and N-cycloheptylthiourea according to Method E and C.

¹H NMR (270 MHz, CHLOROFORM-D) δ ppm 1.39-1.84 (m, 9 H), 1.88-2.06 (m, 2 H), 3.39-3.54 (m, 1 H), 3.64 (s, 2 H), 3.97 (s, 1 H), 4.75 (s, 1 H), 7.84-7.95 (m, 1 H), 8.34 (d, J=7.67 Hz, 1 H), 8.75 (d, J=5.07 Hz, 1 H), 9.10 (s, 1 H). MS (ESI+) for C₁₆H₂₁N₃OS m/z 304 (M+H)⁺

Example 41 5-Isopropyl-2-[(2-methylphenyl)amino]-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-methylphenyl)thiourea and ethyl 2-bromo-3-methylbutanoate according to Method C.

¹H NMR (400 MHz, DMSO-d₆) δ 0.84 (d, J=6.6 Hz, 3 H), 0.88 (d, J=7.0 Hz, 3 H), 2.10 (s, 3 H), 2.34 (m, 1 H), 4.32 (d, J=3.4 Hz, 1 H), 6.83 (d, J=7.8 Hz, 1 H), 7.03 (m, 1 H), 7.16 (m, 1 H), 7.21 (d, J=7.6 Hz, 1 H). MS (ESI+) for C₁₃H₁₆N₂OS m/z 249 (M+H)⁺.

Example 42 2-(Cyclooctylamino)-5,5-dimethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from ethyl-2-bromo-2-methylpropanoate and N-cyclooctylthiourea according to Method C1.

¹H NMR (270 ^(MHz), DMSO-d₆) δ ppm 1.46 (s, 3H), 1.47 (s, 3H), 1.81-1.43 (m, 15H). MS (EI+) for C₁₃H₂₂N₂OS m/z 255 (M+H)^(+.)

Example 43 2-(Cyclooctylamino)-5-isopropyl-1,3-thiazol-4(5H)-one

Synthesis was performed from 2-bromo-3-methylbutyric acid and N-cyclooctylthiourea according to Method C1.

¹H NMR (270 MHz, METHANOL-d4) Major isomer: δ ppm 0.85 (d, J=6.68 Hz, 3 H), 1.01 (d, J=6.93 Hz, 3 H), 1.44-1.91 (m, 14 H), 2.36-2.52 (m, 1 H), 3.98-4.12 (m, 1 H), 4.36 (d, J=3.71 Hz, 1 H). MS (EI+) for C₁₄H₂₄N₂OS m/z 269 (M+H)^(+.)

Example 44 2-(Bicyclo[2.2.1]hept-2-ylamino)-1-thia-3-azaspiro[4.5]dec-2-en-4-one

Synthesis was performed from N-bicyclo[2.2.1]hept-2-ylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D.

¹H NMR (400 MHz, CDCl₃) δ 1.12-2.44 (m, 21 H), 3.34 (m, 1 H).

MS (ESI+) for C₁₅H₂₂N₂OS m/z 279 (M+H)^(+.)

Example 45 2-(Tricyclo[3.3.1.0˜3,7˜]non-3-ylamino)-1-thia-3-azaspiro[4.5]dec-2-en-4-one

Synthesis was performed from N-tricyclo[3.3.1.0˜3,7˜]non-3-ylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D.

¹H NMR (400 MHz, CDCl₃) δ 1.24-2.19 (m, 20 H), 2.30 (m, 0.5 H, minor rotamer), 2.41 (m, 1.5 H, major rotamer), 2.53 (m, 0.25 H, minor rotamer), 2.75 (m, 0.75 H, major rotamer).

MS (ESI+) for C₁₇H₂₄N₂OS m/z 305 (M+H)^(+.)

Example 46 2-(Cycloheptylamino)-1-thia-3-azaspiro[4.5]dec-2-en-4-one

Synthesis was performed from N-cycloheptylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D.

¹H NMR (400 MHz, CDCl₃) δ 1.24-2.14 (m, 23 H), 3.48 (m, 1 H).

MS (ESI+) for C₁₅H₂₄N₂OS m/z 281 (M+H)^(+.)

Example 47 2-(Cyclooctylamino)-1-thia-3-azaspiro[4.5]dec-2-en-4-one

Synthesis was performed from N-cyclooctylthiourea and methyl 1-bromocyclohexanecarboxylate according to Method D.

¹H NMR (400 MHz, CDCl₃) δ 1.24-2.13 (m, 25 H), 3.55 (m, 1 H).

MS (ESI+) for C₁₆H₂₆N₂OS m/z 295 (M+H)^(+.)

Example 48 2-{[1-(4-Chlorophenyl)cyclobutyl]amino}-5-isopropyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[1-(4-chlorophenyl)cyclobutyl]thiourea and ethyl 2-bromo-3-methylbutanoate according to Method D.

¹H NMR (400 MHz, DMSO-d₆) δ 0.60 (d, J=6.5 Hz, 0.75 H, minor rotamer), 0.68 (d, J=6.6 Hz, 2.25 H, major rotamer), 0.82 (d, J=6.8 Hz, 0.75 H, minor rotamer), 0.92 (d, J=6.8 Hz, 2.25 H, major rotamer), 1.77-1.87 (m, 1 H), 1.93-2.03 (m, 1 H), 2.21-2.33 (m, 1 H), 2.42-2.65 (m, 4 H, obscured by solvent signal), 4.14 (d, J=3.5 Hz, 0.25 H, minor rotamer), 0.68 (d, J=3.7 Hz, 0.75 H, major rotamer), 7.38 (m, 3 H, major rotamer), 7.45 (m, 1 H, minor rotamer), 9.87 (s, 1 H).

MS (ESI+) for C₁₆H₁₉ClN₂OS m/z 323 (M+H)^(+.)

Example 49 6-{[1-(4-Chlorophenyl)cyclobutyl]amino}-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Synthesis was performed from N-[1-(4-chlorophenyl)cyclobutyl]thiourea and ethyl 1-bromocyclobutanecarboxylate according to Method D.

¹H NMR (400 MHz, DMSO-d₆) δ 1.73-2.12 (m, 4 H), 2.32-2.60 (m, 8 H, obscured by solvent signal), 7.39 (m, 3.3 H, major rotamer), 7.44 (m, 0.7 H, minor rotamer), 9.83 (s, 1 H).

MS (ESI+) for C₁₆H₁₇ClN₂OS m/z 321 (M+H)^(+.)

Example 50 2-(cycloheptylamino)-5,5-diethyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-cycloheptylthiourea and 2-ethylbutyric acid according to Method J and D.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.89-1.01 (m, 6 H), 1.40-2.09 (m, 16 H), 3.44-3.55 (m, 1 H).

MS (ESI+) for C₁₄H₂₄N₂OS m/z 269 (M+H)⁺

Example 51 (5S)-5-isopropyl-2-{[(2S)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2S)-2-phenylpropyl]thiourea and 2-bromo-3-methylbutyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.54-0.85 (m, 3 H), 0.84-1.08 (m, 3 H), 1.08-1.37 (m, 3 H), 2.18-2.43 (m, 1 H), 2.91-3.22 (m, 1 H), 3.27-3.47 (m, J=7.30 Hz, 1 H), 3.44-3.62 (m, 1 H), 4.18-4.37 (m, 1 H), 6.95-7.43 (m, 5 H), 9.26 (s, 1 H, N—H).

MS (ESI+) for C₁₅H₂₀N₂OS m/z 277 (M+H)^(+.)

Example 52 (5R)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2S)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.51-0.70 (m, 3 H), 1.10-1.36(m, 3 H), 1.45-1.80(m, 1 H), 3.11-3.34(m, 1 H), 3.65-3.84(m, 2 H), 3.80-4.07 (m, 1 H), 4.30-4.48 (m, 1 H), 7.10-7.41 (m, 5 H).

MS (ESI+) for C₁₄H₁₈N₂OS m/z 263 (M+H)⁺.

Example 53 (5S)-5-ethyl-2-{[(2S)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2S)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.73-0.97 (m, 3 H), 1.10-1.35 (m, 3 H), 1.53-1.82 (m, 1 H), 1.83-2.11 (m, 1 H), 2.92-3.13 (m, 1 H), 3.48-3.67 (m, 2 H), 4.10-4.32 (m, 1 H), 7.09-7.45 (m, 5 H), 9.27 (s, 1 H, N—H).

MS (ESI+) for C₁₄H₁₈N₂OS m/z 263 (M+H)^(+.)

Example 54 (5R)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-3-methylbutyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.50-0.80 (m, 3 H), 0.84-1.06 (m, 3 H), 1.09-1.32 (m, 3 H), 2.22-2.43 (m, 1 H), 2.91-3.19 (m, 1 H), 3.27-3.45 (m, 2 H), 4.14-4.38 (m, 1 H), 7.07-7.44 (m, 5 H), 9.25 (s, 1 H, N—H).

MS (ESI+) for C₁₅H₂₀N₂OS m/z 277 (M+H)⁺.

Example 55 (5S)-5-isopropyl-2-{[(2R)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-3-methylbutyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.40-0.58 (m, J=6.68 Hz, 3 H), 0.71-0.87 (m, 3 H), 1.03-1.29 (m, 3 H), 2.11-2.24 (m, 1 H), 3.62-3.81 (m, 2 H), 3.83-4.03 (m, 1 H), 4.36-4.51 (m, 1 H), 7.10-7.41 (m, 5 H).

MS (ESI+) for C₁₅H₂₀N₂OS m/z 277 (M+H)^(+.)

Example 56 (5R)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.75-0.97 (m, 3 H), 1.05-1.35 (m, 3 H), 1.58-1.82 (m, 1 H), 1.82-2.05 (m, 1 H), 2.92-3.17 (m, 1 H), 3.44-3.65 (m, 2 H), 4.12-4.36 (m, 1 H), 7.09-7.49 (m, 5 H), 9.26 (s, 1 H).

MS (ESI+) for C₁₄H₁₈N₂OS m/z 263 (M+H)⁺.

Example 57 (5S)-5-ethyl-2-{[(2R)-2-phenylpropyl]amino}-1,3-thiazol-4(5H)-one

Synthesis was performed from N-[(2R)-2-phenylpropyl]thiourea and 2-bromo-butyric acid according to Method D3.

¹H NMR (270 MHz, DMSO-d₆) the major rotamer δ ppm 0.53-0.74 (m, J=7.30, 7.30 Hz, 3 H), 1.08-1.33 (m, 3 H), 1.43-1.63 (m, 1 H), 1.62-1.89 (m, 1 H), 3.13-3.36 (m, 1 H), 3.66-3.86 (m, J=13.61, 7.17 Hz, 1 H), 3.83-4.04 (m, 1 H), 4.26-4.51 (m, J=4.95 Hz, 1 H), 7.09-7.44 (m, 5 H).

MS (ESI+) for C₁₄H₁₈N₂OS m/z 263 (M+H)^(+.)

Example 58 2-Anilino-5-isopropyl-1,3-thiazol-4(5H)-one

Synthesis was performed from N-phenylthiourea and ethyl 2-bromo-3-methylbutanoate according to Method C.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.00 (s, 6 H), 2.40-2.73 (m, 1 H), 4.04-4.34 (m, 1 H), 7.01-7.56 (m, 6 H); MS [M+H]⁺ m/z=235.

Example 59 5-Isopropyl-2-[(2-morpholin-4-ylethyl)amino]-1,3-thiazol-4(5H)-one

Synthesis was performed from N-(2-morpholin-4-ylethyl)thiourea and ethyl 2-bromo-3-methylbutanoate according to Method C.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.70-1.25 (m, 8 H), 2.58 (s, 1 H), 2.78-4.09 (m, 10 H), 4.18-4.54 (m, 1 H); MS [M+H]⁺ m/z=272.

Example 60 2-(Bicyclo[2.2.1]hept-2-ylamino)-1-thia-3-azaspiro[4.4]non-2-en-4-one Example 61 2-(Cycloheptylamino)-1-thia-3-azaspiro[4.4]non-2-en-4-one Example 62 2-(Cyclooctylamino)-1-thia-3-azaspiro[4.4]non-2-en-4-one Example 63 2-[(2,2,3,3-Tetramethylcyclopropyl)amino]-1-thia-3-azaspiro[4.4]non-2-en-4-one

Examples 60-63 were prepared using one of the methodologies described above.

Example 64 2-[(2-chlorobenzyl)amino]-5-isopropyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and 2-Chlorobenzylamine according to Method G+H.

¹H NMR (400 MHz, DMSO-d6) δ ppm 0.62 (d, J=6.84 Hz, 0.75 H), 0.82 (d, J=6.84 Hz, 2.25 H), 0.90 (d, J=6.96 Hz, 0.75 H), 0.99 (d, J=6.84 Hz, 2.25 H), 1.97-2.13 (m, 1 H), 4.41-4.50 (m, 0.5 H), 4.51-4.56 (m, 1.5 H), 4.59 (d, J=3.66 Hz, 0.25 H), 4.63 (d, J=3.66 Hz, 0.75 H), 7.30-7.41 (m, 3 H), 7.45-7.49 (m, 1 H), 9.30 (s, 1 H).

MS (ESI+) for C13H15ClN2O2 m/z 267 (M+H)⁺

Example 65 2-[(4-chlorobenzyl)amino]-5-isopropyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and 4-Chlorobenzylamine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.63 (d, J=6.84 Hz, 0.75 H), 0.80 (d, J=6.84 Hz, 2.25 H), 0.90 (d, J=6.96 Hz, 0.75 H), 0.98 (d, J=6.84 Hz, 2.25 H), 1.96-2.13 (m, 1 H), 4.37-4.41 (m, 0.5 H), 4.44 (d, J=6.10 Hz, 1.5 H), 4.58 (d, J=3.54 Hz, 0.25 H), 4.61 (d, J=3.78 Hz, 0.75 H), 7.27-7.34 (m, 2 H), 7.37-7.45 (m, 2 H), 9.28 (t, J=5.98 Hz, 0.75 H) 9.49 (s, 0.25 H).

MS (ESI+) for C₁₃H₁₅ClN₂O₂ m/z 267 (M+H)⁺

Example 66 5-isopropyl-2-[(2,2,6,6-tetramethylpiperidin-4-yl)amino]-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and 4-amino-2,2,6,6-tetramethylpiperidine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.78-0.84 (m, 3 H), 0.95-1.04 (m, 3 H), 1.33-1.43 (m, 12 H), 1.44-1.58 (m, 2 H), 1.91-2.16 (m, 3 H), 3.96-4.09 (m, 1 H), 4.60 (d, J=3.78 Hz, 0.9 H), 4.84 (d, J=4.03 Hz, 0.1 H), 7.83 (d, J=11.60 Hz, 0.75 H), 8.16 (s, 0.25 H), 8.76 (d, J=11.48 Hz, 1 H), 9.00 (d, J=7.45 Hz, 1 H). MS (ESI+) for C₁₅H₂₇N₃O₂ m/z 282 (M+H)⁺

Example 67 5-isopropyl-2-morpholin-4-yl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and morpholine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.81 (d, J=6.84 Hz, 2 H), 0.87 (d, J=6.84 Hz, 1 H), 0.97-1.01 (m, 3 H), 2.02-2.17 (m, 1 H), 3.06-3.13 (m, 2 H), 3.53-3.77 (m, 6 H), 4.66 (d, J=3.91 Hz, 0.67 H), 4.84 (d, J=4.15 Hz, 0.33 H). MS (ESI+) for C₁₀H₁₆N₂O₃ m/z 213 (M+H)⁺

Example 68 5-isopropyl-2-[(2-morpholin-4-ylethyl)amino]-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and N-(2-aminoethyl)morpholine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.87 (d, J=6.84 Hz, 1 H), 0.92 (d, J=6.84 Hz, 2 H), 1.02 (d, J=6.96 Hz, 3 H), 2.01-2.24 (m, 1 H), 2.63-2.72 (m, 2 H), 2.72-2.81 (m, 1 H), 3.03 (t, J=6.41 Hz, 1 H), 3.08-3.36 (m, 3 H), 3.54-3.67 (m, 1 H), 3.65-3.71 (m, 2 H), 3.75-3.86 (m, 2 H), 4.57 (d, J=4.15 Hz, 0.5 H), 4.82 (d, J=4.39 Hz, 0.5 H), 7.32-8.39 (m, 1 H). MS (ESI+) for C₁₂H₂₁N₃O₃ m/z 256 (M+H)⁺

Example 69 2-(4-benzylpiperidin-1-yl)-5-isopropyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and 4-benzylpiperidine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.76-0.82 (m, 2.25 H), 0.87 (d, J=6.84 Hz, 0.75 H), 0.95-1.01 (m, 3 H), 1.07-1.35 (m, 2 H), 1.60-1.88 (m, 3 H), 2.00-2.18 (m, 1 H), 2.53 (d, J=7.08 Hz, 2 H), 2.74-2.86 (m, 0.5 H), 2.95-3.10 (m, 1.5 H), 3.23 (d, J=12.57 Hz, 0.5 H), 4.03 (d, J=13.55 Hz, 0.75 H), 4.10 (d, J=13.18 Hz, 0.75 H), 4.62 (d, J=3.78 Hz, 0.75 H), 4.84 (d, J=4.15 Hz, 0.25 H), 7.15-7.22 (m, 3 H), 7.24-7.32 (m, 2 H). MS (ESI+) for C₁₈H₂₄N₂O₂ m/z 301 (M+H)⁺

Example 70 2-azocan-1-yl-5-isopropyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and heptamethyleneimine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.80 (d, J=6.84 Hz, 3 H), 1.00 (d, J=6.96 Hz, 3 H), 1.32-1.43 (m, 1 H), 1.47-1.56 (m, 5 H), 1.67-1.76 (m, 4 H), 2.04-2.13 (m, 1 H), 3.37-3.47 (m, 2 H), 3.58-3.71 (m, 2 H), 4.64 (d, J=3.54 Hz, 1 H). MS (ESI+) for C₁₃H₂₂N₂O₂ m/z 239 (M+H)⁺

Example 71 2-[(cyclohexylmethyl)amino]-5-phenyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-phenyl-1,3-oxazol-4(5H)-one and aminomethylcyclohexane according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.92 (m, 2 H), 1.14 (m, 3 H), 1.57 (m, 6 H), 3.14 (m, 2 H), 5.72 (s, 0.7 H), 5.74 (s, 0.3 H), 7.28 (m, 2 H), 7.39 (m, 3 H), 9.00 (t, J=5.74 Hz, 0.7 H), 9.25 (s, 0.3 H). MS (ESI+) for C₁₆H₂₀N₂O₂ m/z 273 (M+H)⁺

Example 72 2-(cycloheptylamino)-5-phenyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-phenyl-1,3-oxazol-4(5H)-one and cycloheptylamine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 1.35-1.70 (m, 10 H), 1.92 (m, 2 H), 3.78 (m, 1 H), 5.69 (s, 0.75 H), 5.73 (s, 0.25 H), 7.28 (m, 2 H), 7.39 (m, 3 H), 8.92 (s, 1 H). MS (ESI+) for C₁₆H₂₀N₂O₂ m/z 273 (M+H)⁺

Example 73 5-benzyl-2-[(cyclohexylmethyl)amino]-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-benzyl-1,3-oxazol-4(5H)-one and aminomethylcyclohexane according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.7-1.7 (m, 11 H), 2.93 (m, 3 H), 3.16 (m, 1 H), 4.95 (m, 1 H), 7.23 (m, 5 H), 8.56 (s, 1 H). MS (ESI+) for C₁₇H₂₂N₂O₂ m/z 287 (M+H)⁺

Example 74 2-(cycloheptylamino)-5-isopropyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and cycloheptylamine according to Method G+H.

¹H NMR (400 MHz, DMSO-d₆) δ ppm 0.77-082 (m, 3 H), 0.94-1.01 (m, 3 H), 1.32-1.67 (m, 10 H), 1.80-1.90 (m, 2 H), 2.00-2.11 (m, 1 H), 3.62-3.74 (m, 1 H), 4.53 (d, J=3.66 Hz, 0.73 H), 4.57 (d, J=3.66 Hz, 0.27 H), 8.80 (d, J=8.06 Hz, 0.73 H), 9.06 (s, 0.23 H). MS (ESI+) for C₁₃H₂₂N₂O₂ m/z 239 (M+H)⁺

Example 75 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and bicyclo[2.2.1]hept-2-amine according to Method G+H.

¹H NMR (400 MHz, ^(DMSO)-d₆) δ ppm 0.75-0.84 (m, 3 H), 0.93-1.02 (m, 3 H), 1.03-1.17 (m, 3 H), 1.34-1.52 (m, 4 H), 1.60-1.71 (m, 1 H), 1.98-2.25 (m, 3 H), 3.46-3.53 (m, 1 H), 4.50-4.58 (m, 1 H), 8.67 (s, 1 H). MS (ESI+) for C₁₃H₂₀N₂O₂ m/z 237 (M+H)⁺

Example 76 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isobutyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isobutyl-1,3-oxazol-4(5H)-one and bicyclo[2.2.1]hept-2-amine according to Method G+H.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.93-1.02 (m, 6 H), 1.08-1.37 (m, 3 H), 1.42-1.97 (m, 8 H), 2.28-2.41 (m, 2 H), 3.55-3.62 (m, 0.8 H), 3.75-3.83 (m, 0.2 H), 4.57-4.63 (m, 0.2 H), 4.68-4.75 (m, 0.8 H), 10.21 (s, 1 H).

MS (ESI+) for C₁₄H₁₇N₃O₃ m/z 251 (M+H)⁺

Example 77 2-(cycloheptylamino)-5-isobutyl-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isobutyl-1,3-oxazol-4(5H)-one and cycloheptylamine according to Method G+H.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.93-1.01 (m, 6 H), 1.37-2.10 (m, 15 H), 3.71-3.82 (m, 0.65 H), 3.92-4.02 (m, 0.35 H), 4.60 (dd, J=10.07, 2.99 Hz, 0.35 H), 4.66 (dd, J=9.89, 3.05 Hz, 0.65 H), 9.38 (s, 1 H).

MS (ESI+) for C₁₄H₁₇N₃O₃ m/z 253 (M+H)⁺

Example 78 5-isobutyl-2-[(2-methylphenyl)amino]-1,3-oxazol-4(5H)-one

Synthesis was performed from 2-amino-5-isopropyl-1,3-oxazol-4(5H)-one and 2-methylphenylamine according to Method G+H.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.93-1.03 (m, 6 H), 1.64-1.76 (m, 1 H), 1.81-1.95 (m, 2 H), 2.35 (s, 3 H), 4.82-4.89 (m, 1 H), 7.22-7.31 (m, 4 H).

MS (ESI+) for C₁₄H₁₇N₃O₃ m/z 247 (M+H)⁺

Example 79 2-(bicyclo[2.2.1]hept-2-ylamino)-5-isopropyl-5-methyl-1,3-thiazol-4(5H)-one

To a solution of 2-amino-2,3-dimethylbutanoic acid (400 mg, 3.05 mmol) and potassium bromide (1.190 g, 10.00 mmol) in H₂O (4 mL) and concentrated H₂SO₄ (345 μL) at 0° C. under stirring was added via a syringe over 50 min a solution of NaNO₂ (295 mg, 4.27 mmol) in H₂O (900 μL). The reaction was allowed to slowly reach ambient temperature, and was then stirred overnight. The resulting solution was extracted with diethyl ether (2×15 mL), and the combined organic phases were washed with brined and dried over MgSO₄. The solvent was removed to give a transparent oil (290 mg), which was used without any further purification. A mixture of the crude oil (250 mg) and N-bicyclo[2.2.1]hept-2-ylthiourea (F18616001) (100 mg, 0.587 mmol) in 1,4-dioxane (600 μL) was stirred at 100° C. in a sealed tube for 3 days. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC chromatography to give the product as a white solid.

¹H NMR (400 MHz, CDCl₃) δ 0.85-0.88 (m, 3 H), 0.99-1.04 (m, 3 H), 1.10-1.27 (m, 4 H), 1.46-1.58 (m, 2 H), 1.61-1.65 (m, 3 H), 1.71-1.88 (m, 2 H), 2.12-2.23 (m, 1 H), 2.27-2.42 (m, 2 H), 3.35 (m, 0.8 H, major isomer), 4.03 (m, 0.2 H, minor isomer).

MS (ESI+) for C₁₄H₂₂N₂OS m/z 267 (M+H)⁺.

General Methodologies K-PP

Methodologies for Synthesis of Starting Materials: Carboxylic Acids, Esters, Acid Chlorides, Acyl Isothiocyanates:

Method K

The thioisocyante intermediates can be prepared by the method K. Formation of the acid chloride, such as by treatment with oxalyl chloride and DMF, or thionyl chloride, followed by treatment with KNCS provides the thioisocyantes. Alternatively, treatment of the carboxylic acid with thionyl chloride, then bromination, such as with Br₂ and PBr₃, followed by treatment with KNCS also provides the thioisocyantes.

Method L

Preparation of bromo substituted esters and carboxylic acids is described in Method L. Bromination of the carboxylic acid, such as with Br₂, PCl₃ (cat.), followed by formation of the acid chloride, such as by treatment with oxalyl chloride or thionyl chloride, and treatment with alcohols, TMSCHN₂ or CH₂N₂, yields the desired compounds. Alternatively, the acid chloride can be formed first, followed by bromination step. Starting from esters, treatment with strong base, e.g. LDA, and a leaving group supplier such as TMSCl, followed by bromination provides the desired esters. Using amino acid starting materials (A=NH₂), bromination, such as by reaction with HBr in the presence of NaNO₂, yields the desired bromo acids.

Method M

Methylation of various substituted acids and esters, such as by treatment with base and an methyl halide, followed by bromination, yields the desired α-bromo-α-methyl compounds.

Method N

Conversion of various ketones to the esters is accomplished by Method N. Treatment with an appropriate dithiane, such as 2-trimethylsilyl-1,3-dithiane, in the presence of base, e.g. n-BuLi, followed by chlorination, such as with N-chlorosuccinimide, yields the desired compounds.

Methodologies for Synthesis of Starting Materials: Thioureas and Amines:

Method O

Formation of the desired thioureas is detailed in Method O. Treatment of amines with BzNCS, followed by deprotection, such as with base, yields the thioureas. Alternatively, the thiourea is formed through treatment with 1,1-thiocarbonyldiimidazole in the presence of base, e.g. NEt₃, followed by treatment with ammonia.

Method P

Alternatively, the thiourea is formed as described in Method P. Treatment of a substituted thioisocyanate with ammonia yields the desired thioureas.

Method Q

Preparation of substituted bicyclo[2.2.1]heptane amines is described in the synthetic scheme in shown in Example 97.

Method R

Preparation of 1-amino-1-methylethyl benzenes is described in Method R. Methylation of cyanomethylbenzenes, such as with treatment with methyl halides in the presence of non-nucleophilic base, e.g. KHMDS, yields the 1-cyano-1-methylethyl benzenes. Oxidation of the cyano compounds, such as with H₂O₂, in the presence of base, e.g. K₂CO₃, yields the amides. Hofmann rearrangement of the amides, such as by treatment with (O₂CCF₃)₂IPh, yields the desired amines.

Method S

Bicyclo[2.2.1]heptanyl thioureas are provided via Method S. Bromination of carboxylic acids, such as with Br₂, PCl₃, and the resulting rearrangement provides the 2-bromo-1-carboxylic acids. Dehalogenation, such as with Zn in AcOH, yields the 1-carboxylic acids. The Curtius rearrangement such as by treatment with DPPA and a base, e.g. NEt₃, and an alcohol provides the protected amine. Deprotection, such as with acid, followed by formation of the thiourea and deprotection, as described above, provides the desired thioureas.

Method T

Base mediated substitution of a nitrophenol with a alkyl halide, provides the nitrophenyl ether. For example Cs₂CO₃ can be used in the presence of NaI. Reduction of the nitro group, such as with H₂ in the presence of a catalyst, e.g. Pd/C, yields the desired amines.

Method U

Method U describes the formation of cyclopropanamines from benzonitriles is accomplished by treatment with EtMgBr in the presence of Ti(Oi-Pr)₄, followed by treatment with BF₃.OEt₂.

Method V

Formation of bicyclo[2.2.2]octanyl amines is described in Method V. De-esterification of the esters, such as with base, e.g. LiOH, followed the Curtius rearrangement as described previously and deprotection, e.g. acid, provides the desired amines.

Method W

Formation of (bicyclo[2.2.1]heptanylmethyl)-thioureas from the carboxylic acids is described in Method W. Formation of the acid chloride, such as by treatment with oxalyl chloride and DMF (cat.), followed by treatment with ammonia or ammonium hydroxide, provides the amide. Reduction of the amide, such as with treatment with LiAlH₄, to the amine, followed by chemistry previously described, yields the desired thioureas.

Methodologies for Synthesis of Final Products:

Method X

Thiazolones can be prepared by many methods, including that described in Method X. Treatment of a bromo-substituted carboxylic acid or ester with thiourea in the presence of base, such as DIEA provides the condensation/ring closure to the desired 2-amino-thiazolones.

Method Y

Alternatively, as shown in Method Y, treatment of a bromo-substituted carboxylic acid with thiourea in the presence of base, such as NaOAc provides the condensation/ring closure to the desired 2-amino-thiazolones.

Method Z

Thiazolones also can be prepared from amines by the method described in Method Z. Coupling of an amine with an isothiocyante, e.g. in the presence of base, such as NEt₃, provides the condensation/ring closure to the desired 2-amino-thiazolones.

Method AA

5,5-Disubstituted thiazolones can be prepared from thiazolones via the method described in Method AA. Treatment first with strong base, e.g. LDA or NaHMDS, then with a compound comprising an appropriate leaving group, such as R^(B)-LG, provides the desired compounds.

Method BB

Similarly, formation of 5-fluoro-thiazolones can be prepared as described in Method BB. Treatment first with strong base, e.g. LDA or NaHMDS, and TMSCl, followed by fluorination, e.g. with Selectfluor, provides the desired compounds.

Method CC

Similarly, formation of 5-trifluoromethyl-thiazolones can be prepared as described in Method CC. Treatment first with strong base, e.g. LDA or NaHMDS, and TMSCl, followed by trifluoromethylation, e.g. with S-(trifluoromethyl)dibenzothiophenium salt, provides the desired compounds.

Method DD

Formation of 5-carboxymethyl-thiazolones or the corresponding esters can be prepared as described in Method DD. Coupling of carboxylic acids with a substituted alkene, such as in the presence of DBU, followed by treatment with base, e.g. LiOH, provides the desired compounds.

Method EE

Formation of 5-spiro-thiazolones can be prepared as described in Method EE. Coupling of the thiazolone in the presence of strong base, e.g. LDA or NaHMDS, provides the desired compounds. Alternatively, the cyclization can be achieved in two steps, alkylation first with base, e.g. HMDS, in the presence of TMSCl; followed by further treatment with base, e.g. LDA, in the presence of a bis-electrophile.

Method FF

Formation of 5-hydroxymethyl-thiazolones can be prepared as described in Method FF. Treatment of a thiazolone with a ketone in the presence of strong base, e.g. LDA or NaHMDS, provides the desired compounds.

Method GG

Formation of 5-fluoromethyl-thiazolones can be prepared as described in Method GG. Fluorination of 5-hydroxymethyl-thiazolones e.g. with DAST or Deoxo-Fluor, provides the desired compounds.

Method HH

The compounds of the invention can be prepared by the method described in this scheme. Alkylation of the racemic thiazalone with a chiral base, such as

where R^(m) and R^(n) are independently selected from alkyl, aryl, and heterocyclyl, where R^(o) and R^(p) are independently selected from aryl, where J is alkyl, O, NH or S, and where M¹ and M² are independently selected from Li, Na, K, Cs, Cu, Zn, and Mg, e.g. a chiral lithium base, more specifically

and an appropriate alkylating agent, such as a alkyl halide (e.g. an alkyl iodide) or sulfonate (e.g., mesylate, triflate), [LG is halide, tosylate, mesylate, triflate, or the like] provides the desired chiral di-substituted thiazolone. Preferably, the alkylation is performed in the presence of amine base, such as TMEDA. Treatment with the R,R form of the base provides the stereochemistry shown when R³ is methyl. Treatment with the S,S form provides the opposite stereochemistry to that shown when R³ is methyl. The reaction is maintained at a temperature below about RT, preferably below about 0° C., more preferably at or below about −15° C. An aprotic solvent, e.g. toluene is acceptable. Method II

Formation of thiazolone amines and ethers can be prepared as described in Method II. Bromination of thiazolones e.g. with NBS or other techniques known to one skilled in the art, followed by treatment with an amine or alcohol, provides the desired compounds.

Method JJ

Formation of thiazolone amines can be prepared from the alcohols as described in Method JJ. Following the procedure for the Dess-Martin Periodinane or Swern reactions, followed reductive amidation, such as with reacting with an amine together with NaBH(OAc)₃ or NaBH₃CN, provides the desired compounds.

Method KK

Alternatively, formation of 5-spiro-thiazolones can be prepared from the furanone as described in Method KK. Treatment of the furanone with a thiourea provides thiazolone alcohol. Protection of the alcohol, such as with dihydropyran in the presence of acid, followed by treatment with strong base, e.g. LDA, and 3-bromo-2-methylprop-1-ene, and deprotection, e.g. with PTSA, and cyclization, such as with acid, provides the desired compounds.

Method LL

Further, formation of 5-spiro-thiazolones can be prepared from the thiazolone as described in Method LL. Treatment of the thiazolone with strong base, e.g. LDA or NaHMDS and alkylation, such as with (2-bromoethoxy)(tert-butyl)dimethylsilane provides the protected thiazolone alcohol. A subsequent round of base and silane provides the disubstituted thiazolone. Deprotection, e.g. with acid, followed with addition of a compound containing an appropriate leaving group, e.g. MsCl, in the presence of base, e.g. DIEA, and cyclization, such as with a substituted amine, provides the desired spiro piperidine compounds.

Method MM

1-Substituted piperidinemethylthiazolones can be prepared by method MM. After deprotection, such as by treatment with acid, treatment with sulfonyl chlorides (R¹²SO₂Cl) in the presence of base, e.g. NEt₃, provides compounds where R^(Q)=SO₂R^(S). Alternatively, after deprotection, treatment with carboxylic acid (R^(R)CO₂H) with standard coupling chemistry, e.g. EDCI, and HOBt, provides compounds where R^(Q)=COR^(R). Alternatively, after deprotection, treatment with active carbonyl compounds, e.g. acid anhydrides (R^(R)CO—O—COR^(R)) in the presence of base, e.g. DIEA, provides compounds where R^(Q)=COR^(R).

Method NN

Formation of 5-spiro-thiazolones can be prepared from the thiazolone as described in Method NN. Treatment of the thiazolone with strong base, e.g. LDA and alkylation, such as with BrCH₂CH₂Br provides the thiazolone bromoethyl compound. Further treatment with strong base, e.g. LDA, and dimethylketone, provides the desired spiro tetrahydrofuryl compounds.

Method OO

Substituted amidomethylthiazolones can be prepared by method OO. Treatment of a substituted thioureas and with active carbonyl compounds, e.g. maleic anhydride in the presence of acid, e.g. AcOH, provides the thiazolone carboxylic acids. Treatment of the acid with an amine, such as in the presence of a coupling reagent, e.g. HATU and base such as DIEA provides the desired amides.

Method PP

Substituted thiazolone esters can be prepared from the alcohol by method PP. Treatment of an alcohol-substituted thiourea with active carbonyl compounds, e.g. an acid chloride, in the presence of base, e.g. DIEA, provides the desired esters.

Separation Methods

Many of the final compounds were separated by two main chromatographic methods. Normal phase liquid chromatography (NPLC) and supercritical fluid chromatography (SFC) were the two techniques utilized. NPLC was performed with Chiralpak AD/AD-H and Chiralcel OJ-H columns. The mobile phase consisted of hexane (0.2% diethylamine (DEA)) and/or methanol, ethanol (0.2% DEA), or isopropanol (0.2% DEA). All separations were conducted at ambient temperatures. Columns used with SFC were the Chiralpak AD-H and AS-H, the Chiralcel OD-H, and the Astec (R,R) P-CAP. The mobile phased was comprised of liquid carbon dioxide and an organic modifier such as methanol (with or without 0.2% DEA), ethanol (with or without 0.2% DEA), isopropanol (with or without 0.2% DEA), or acetonitrile (with or without 0.2% DEA). Organic modifiers were used individually with liquid carbon dioxide or in combinations with each other and the liquid carbon dioxide. Column/oven temperature was between 35 and 40° C., and the outlet pressure was either 100 or 120 bar.

Illustrative Method for Separating Enantiomers of Thioureas:

Stationary phase: ChiralPAK-AD, 20u, from Chiral Technology

Column: MODCOL spring load column, 4″×30 cm containing of 2.0 kg of stationary phase.

Mobile phase: 100% MeOH

Flow rate: 500 ml/min

Temperature: 30° C.

Detection wavelength: 230 nm

Abbreviations

AIBN, 2,2′-Azobisisobutyronitrile

aq., aqueous

brine, a saturated solution of NaCl in water

conc., concentrated

DAST, Diethylaminosulfur trifluoride

DBU, 1,8-Diazabicyclo[5.4.0]undec-7-ene

DCM, dichloromethane

DEAD, diethyl azodicarboxylate

Deoxo-Fluor, Bis(2-methoxyethyl)aminosulfur trifluoride

Dess-Martin Periodinane, 1,1,1-Tris(acetyloxy)-1,1-dihydro-1,2-benziodoxol-3(1H)-one

DIEA, N,N-Diisopropylethylamine

DMF, N,N-Dimethylformamide

DPPA, Diphenylphosphoryl azide

EDCI, 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride

EtOAc, ethyl acetate

EtOH, ethanol

HOBT, 1-Hydroxy-1H-benzotriazole

Hunig's base, N,N-Diisopropylethylamine

KHMDS, Potassium bis(trimethylsilyl)amine

LDA, Lithium diisopropylamide

LiHMDS, Lithium bis(trimethylsilyl)amine

MeOH, methanol

(R)-MOP, (R)-(+)-2-(diphenylphosphino)-2′-methoxy-1,1′-binaphthyl

MS; Mass Spectrum

MsCl, Methanesulfonyl chloride

MTBE, methyl tert-butyl ether

MW, microwave

NaHMDS, Sodium bis(trimethylsilyl)amine

NBS, N-Bromosuccinimide

n-BuLi, n-Butyllithium

PCC, Pyridinium chlorochromate

i-PrOH, iso-propanol

PTSA, p-toluenesulfonic acid

r.t., room temperature

sat'd, saturated solution in water

Selectfluor™, N-Fluoro-N′-chloromethyltriethylenediamine bis(tetrafluoroborate)

TBDMS, tert-butyl dimethylsilyl

THF, Tetrahydrofuran

TLC, thin layer chromatography

TMSCl, chlorotrimethylsilane

Synthesis of Starting Materials: Carboxylic Acids, Esters, Acid Chlorides, and Acyl Isothiocyanates (Procedures Method-L, Method-M, Method-N, Method-K).

Unless otherwise noted, all materials were obtained from commercial suppliers and used without further purification. All parts are by weight and temperatures are in degrees centigrade unless otherwise indicated. All microwave-assisted reactions were conducted with a Smith Synthesizer from Personal Chemistry, Uppsala, Sweden or a Discover Instrument from CEM, Matthews, N.C. All compounds showed NMR spectra consistent with their assigned structures. Melting points were determined on a Buchi apparatus and are uncorrected. Mass spectral data was determined by electrospray ionization technique. All examples were purified to >95% purity as determined by high-performance liquid chromatography. Unless otherwise stated, reactions were run at RT.

Example 80 (S)-2-Bromo-3-methylbutanoic acid

Method L

A 2 L jacketed reactor was charged with toluene (150 mL), water (150 mL) and 48% hydrobromic acid (260 mL, 2.30 mol). To this stirred, two-phase solution at 0° C., was added L-valine (96.2 g, 0.82 mol) in one portion (a mild exotherm was observed, temperature rose to 3.5° C.). The mixture was further cooled to −5° C., whereupon an aqueous solution of sodium nitrite (73.7 g, 1.07 mol) was added drop-wise over 6 h. The solution turned dark brown. Once the sodium nitrite was completely added, the reaction mixture was stirred for an additional 3 h at −5° C. Then, the reaction mixture was diluted with toluene (250 mL), warmed to 20° C., and stirred for 12 h. The organic layer was separated and the aqueous layer was extracted with toluene (300 mL). The toluene layers were combined and washed with a 20% sodium thiosulfate solution (200 mL) (virtually all color disappeared) followed by a 20% NaCl solution (200 mL). The organic layer was separated, and the solvent was concentrated in vacuo, and then placed on the high vacuum pump for 4 h to afford the title compound (107 g) as a pale yellow crystalline solid. MS (ESI, pos. ion) m/z: 179.1/180.9.

Example 81 1-Bromocyclopentanecarboxylic acid

Method L

Phosphorus trichloride (0.54 mL, 6.20 mmol) was added drop-wise to the mixture of cyclopentanecarboxylic acid (14.2 g, 124 mmol) and bromine (7.35 mL, 143 mmol). The mixture was then gradually heated to 85° C. and stirred at this temperature in a sealed vessel for 12 h. After cooling to ambient temperature, the mixture was partitioned between EtOAc and water. The organic portion was separated, washed with water and brine, and conc. in vacuo to give the title compound as a white solid.

Example 82 Ethyl 1-bromocyclopentanecarboxylate

DMF (a few drops) was added to a mixture of 1-bromocyclopentane-carboxylic acid (23.9 g, 124 mmol) and oxalyl chloride (11.6 mL, 130 mmol) in 250 mL of CH₂Cl₂. The mixture was stirred at ambient temperature for 2 h. After removing the low-boiling solvents in vacuo, ethanol (50 mL) was added to the residue followed by the addition of N,N-diisopropylethylamine (22.7 mL, 130 mmol). The mixture was stirred at ambient temperature for 20 min. After removing the low-boiling solvents in vacuo, the residue was partitioned between diethyl ether and water. The organic portion was washed with water and brine, and conc. in vacuo. The crude product was filtered through a plug of silica gel using 0 to 10% EtOAc in hexanes as the eluant. The title compound was obtained as a pale oil.

Example 83 Methyl 2-bromo-2-cyclohexylacetate

Method L

A 100 mL round-bottomed flask was charged with cyclohexylacetic acid (5.0 g, 0.035 mol) and thionyl chloride (4.92 g, 3.0 mL, 0.041 mol). This solution was heated to reflux during which time gas evolution occurred. After 1 h at 80° C., bromine (7.03 g, 2.25 mL, 0.044 mol) and phosphorus tribromide (0.350 mL) were added. The reaction temperature was maintained at 80° C. until the color faded from dark red to a light pink (˜2 h) after which time MeOH (5.0 mL) was added, and the reaction mixture was refluxed for 30 min more. After cooling to room temperature, sodium thiosulfate was added, the suspension was filtered, and then concentrated in vacuo to provide the title compound. This bromo-ester was used without any further purification.

Example 84 Methyl 2-bromo-2-(tetrahydro-2H-pyran-4-yl)acetate

Method L

A 250 mL round-bottomed flask was charged with 2-(tetrahydro-2H-pyran-4-yl)acetic acid (5.0 g, 0.035 mol) and 100 mL of MeOH. To this solution was added 5 drops of conc. H₂SO₄. This mixture was heated at reflux for 12 h, after which time the MeOH was removed in vacuo. The remaining residue was dissolved in EtOAc, washed with saturated aqueous NaHCO₃, dried, and concentrated in vacuo to give the desired methyl ester. This compound was used directly in the next step without further purification.

To a dry 250 mL round-bottomed flask was added 2.20 g of methyl 2-(tetrahydro-2H-pyran-4-yl)acetate (0.014 mol) and 100 mL of dry THF. This solution was cooled to −78° C. and LDA (2.0 M in THF/heptane/ethyl benzene, 10.4 mL, 0.021 mol) was added. The resulting brown solution was stirred at −78° C. for 45 min. TMSCl (3.22 g, 3.5 mL, 0.028 mol) was then added at −78° C., and the reaction mixture was then warmed to room temperature. After being re-cooled to −78° C., N-bromosuccinimide (4.94 g, 0.028 mol) was added to the reaction mixture, and the resulting suspension was allowed to slowly warm to room temperature where it continued to stir for an additional 1.5 h. The suspension was then filtered thru a pad of SiO₂ using diethyl ether as the eluant. Purification of the filtrate by column chromatography (SiO₂ gel, 10:1 to 4:1 hexanes/ethyl acetate) delivered the desired α-bromo ester, which was used in subsequent steps without further purification.

Example 85 Ethyl 2-(pyridin-4-yl)propanoate

Method M

To a solution of LiN(TMS)₂ (Aldrich, 1.0 M solution in THF, 30 mL, 30 mmol) in THF (30 mL) was added ethyl 4-pyridylacetate (Aldrich, 4.7 mL, 30 mmol) at 0° C. Methyl iodide (Aldrich, 2.4 mL, 38 mmol) was added 30 min later. After 1 h, the reaction mixture was concentrated in vacuo. The crude product was purified by silica gel chromatography. Mass Spec. m/z+ion 180 (M+1).

Example 86 Ethyl 2-bromo-2-(pyridin-4-yl)propanoate

The above compounds were prepared according to the procedure reported in the literature: see D. Yang, J. Org. Chem. 2002, 67, 7429. MS: 258, 260 (M+1). To a solution of ethyl 2-(pyridin-4-yl)propanoate (5.3 g, 30 mmol), Mg(ClO₄)₂ (Aldrich, 2.0 g, 9.0 mmol) in CH₃CN (60 mL) was added N-bromosuccinimide (Aldrich, 5.9 g, 33 mmol) at room temperature. After 2 h, the reaction mixture was diluted with ether (200 mL), and 10% Na₂CO₃. The organic phase was separated, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. Mass Spec. m/z+ion 258, 260 (M+1).

Example 87 Ethyl 2-bromo-2-(pyridin-3-yl)propanoate

To a stirred mixture of ethyl 2-(pyridin-3-yl)propanoate (4.2 g, 23 mmol), CCl₄ (100 mL), and N-bromosuccinimide (Aldrich, 4.6 g, 26 mmol) was added 2,2′-azobisisobutyronitrile (Aldrich, 0.8 g, 5 mmol) under N₂ at room temperature. The mixture was gradually heated to reflux. After 7 h, the reaction mixture was concentrated in vacuo. The crude was purified by silica gel chromatography. Mass Spec. m/z+ion 258, 260 (M+1).

Example 88 4-(1,3-Dithian-2-ylidene)-6-fluoro-3,4-dihydro-2H-chromene

Method N

To a solution of 2-trimethylsilyl-1,3-dithiane (5.10 g, 26.5 mmol) in 50 mL of anhydrous THF at −60° C. under N₂ was added drop-wise n-BuLi (1.6 M solution in hexanes, 16.6 mL, 26.5 mmol). The mixture was left to warm slowly to 0° C. over 3 h and subsequently cooled to −60° C. A solution of 6-fluoro-2,3-dihydrochromen-4-one (4.40 g, 26.5 mmol) in 25 mL of THF was added drop-wise. The mixture was slowly warmed to ambient temperature overnight, then poured into water, and extracted with EtOAc. The combined organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 10% of EtOAc in hexanes). The title compound was obtained as a pale oil.

Example 89 Ethyl 4-chloro-6-fluoro-3,4-dihydro-2H-chromene-4-carboxylate

A solution of 4-(1,3-dithian-2-ylidene)-6-fluoro-3,4-dihydro-2H-chromene (4.60 g, 17.1 mmol) in 45 mL of anhydrous THF in an addition funnel was added drop-wise to a stirring solution of N-chlorosuccinimide (11.7 g, 85.7 mmol) in 100 mL of CH₃CN and 50 mL of EtOH at r.t. After 3 h, 50 mL of water was added. The mixture was partitioned between EtOAc and water. The combined organic portions were washed with brine, and conc. in vacuo. The residue was purified by flash column chromatography (0 to 10% of EtOAc in hexanes). The title compound was obtained as a colorless oil.

Example 90 (R-2-Bromo-3-methylbutanoyl chloride

Method K

To a 500 mL round-bottom flask was added 5.0 g (27.6 mmol) of (R)-2-bromo-3-methylbutanoic acid and 200 mL CH₂Cl₂. The resulting solution was cooled to 0° C. in an ice bath and then 3 mL of oxalyl chloride (34.4 mmol) was added in one portion. After 5 min, 0.2 mL of DMF (2.59 mmol) was added drop-wise. Once the addition was completed, the mixture was warmed to room temperature and stirred for 4 h. The mixture was then concentrated, triturated with hexanes (50 mL), and filtered. The residual solid was washed with hexane (2×10 mL) and the combined supernatant liquids were concentrated to afford the title compound as a pale yellow oil.

Example 91 (R)-2-Bromo-3-methylbutanoyl isothiocyanate

A 100 mL round-bottom flask was charged with KNCS (0.786 g, 8.08 mmol). Acetone (24 mL) was added and the mixture stirred at room temperature until the solid was completely dissolved. A solution of (R)-2-bromo-3-methylbutanoyl chloride (1.51 g, 7.55 mmol, 1.0 equiv) in acetone (2 mL) was added drop-wise resulting in the formation of a white precipitate with concomitant color change of the solution from clear to pink to reddish orange. Once addition was complete, the mixture was stirred for 30 min at room temperature. The reaction mixture was then filtered through Celite in a sintered glass (medium porosity) funnel, and washed twice with acetone (10 mL each wash). The deep red solution was concentrated, taken up in hexanes (40 mL), and re-filtered. Concentration afforded the title compound as an orange oil.

Synthesis of Starting Materials: Thioureas and Amines (Procedures: Method-O, Method-P, Method-Q, Method-R, Method-S, Method-T, Method-U, Method-V, Method-W).

Example 92 (±)-endo-1-(Bicyclo[2.2.1]heptan-2-yl)thiourea

Method O

To a stirred solution of 1,1-thiocarbonyldiimidazole (1.94 g, 10.9 mmol) and triethylamine (3.0 mL, 21.8 mmol) in dichloromethane (22.0 mL) under nitrogen was added (±)-endo-2-aminonorborane HCl (1.21 g, 10.9 mmol) over 10 min at ambient temperature for 3 h. The solvent was then evaporated in vacuo, and the residue was dissolved in a 0.5M solution of ammonia in dioxane. After stirring at room temperature under nitrogen for 16 h, the resulting solid was filtered off, and the filtrate was evaporated in vacuo. Upon scratching the glass, the residue crystallized. The solid was placed on the high vacuum pump overnight to afford the title compound (1.16 g) as a brown crystalline solid. MS (ESI, pos. ion) m/z: 171.2 (M+H).

Example 93 1-Benzoyl-3-cyclooctylthiourea

Method O

Benzoyl isothiocyanate (7.40 mL, 54.0 mmol) was added to a solution of cyclooctanamine (6.25 g, 49.1 mmol) in 200 mL of chloroform. The mixture was stirred at ambient temperature overnight. The solvents were removed in vacuo to give the title compound as a viscous light yellowish oil. MS m/z: 291.0 (M+H)⁺.

Example 94 1-Cyclooctylthiourea

A mixture of 1-benzoyl-3-cyclooctylthiourea (14.3 g, 49.1 mmol) and potassium carbonate (34.6 g, 250 mmol) in methanol (200 mL), water (100 mL), and THF (100 mL) was stirred at ambient temperature overnight. The low boiling solvents were removed in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was washed with brine, and concentrated in vacuo. The title compound was obtained as a white solid after flash column chromatography (0 to 100% of ethyl acetate in hexanes). MS m/z: 187.1 (M+H)⁺.

Example 95 (±)-exo-1-(Bicyclo[2.2.1]heptan-2-yl)thiourea

Method P

A solution of exo-2-norbornylisothiocyanate (32.2 mL, 326 mmol) in 0.5M solution of ammonia in dioxane (1.3 L, 652 mmol) in a 2 L round-bottomed flask was stirred at room temperature for 16 h. The solvent was then evaporated in vacuo, and the solid was further dried under high vacuum to afford the title compound (39.0 g) as a white amorphous solid. MS (ESI, pos. ion) m/z: 171.2 (M+H).

Example 96 1-Adamantylthiourea

Method P

A mixture of 1-adamantyl isothiocyanate (4.83 g, 25.0 mmol, Aldrich) and ammonia (0.5 M solution in 1,4-dioxane, 100 mL, 50 mmol) was stirred at ambient temperature for 48 h. The solvents were removed in vacuo to give the title compound as a white solid. MS m/z: 211.1 (M+H)⁺.

Example 97

(1R,2S,4R,5S)-2,5-Bis(trichlorosilyl)-bicyclo[2.2.1]heptane

Method Q

A solution of allylpalladium(II) chloride (0.0180 g, 0.0492 mmol) and (R)-(+)-2-(diphenylphosphino)-2′-methoxy-1,1′-binaphthyl (0.105 g, 0.223 mmol) in benzene (2.5 mL) was placed into a double-jacketed 250-mL three-neck flask equipped with a mechanical stirrer under nitrogen atmosphere. Trichlorosilane (20.0 mL, 198 mmol) was added, and the mixture was cooled to −3° C. Bicyclo[2.2.1]hepta-2,5-diene (8.3 mL, 76.9 mmol) was added slowly with mechanical stirring. After stirring at −3° C. for 69 h, the color of the mixture turned into a pale yellowish solid. The reaction mixture was dissolved in toluene (anhydrous, 60 mL), and then concentrated in vacuo to give a pale solid, which was used in the following reaction without further purification.

Example 98 (1R,2S,4R,5S)-2,5-Bis(trimethoxysilyl)bicyclo[2.2.1]heptane

A mixture of methanol (anhydrous, 60 mL), triethylamine (anhydrous, 80 mL), and diethyl ether (anhydrous, 50 mL) was added slowly to (1R,2S,4R,5S)-2,5-bis(trichlorosilyl)-bicyclo[2.2.1]heptane (crude from the previous reaction, 76.9 mmol) in diethyl ether (anhydrous, 50 mL) at 0° C. under a nitrogen atmosphere. After the mixture was stirred at ambient temperature overnight, the precipitated salts were removed by filtration. The solids were washed with diethyl ether (50 mL×3). The combined filtrates were concentrated in vacuo to yield a light yellow slurry which was used in the next reaction without further purification.

Example 99 (1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diol

To (1R,2S,4R,5S)-2,5-bis(trimethoxysilyl)bicyclo[2.2.1]heptane (76.9 mmol) was added potassium hydrogen fluoride (33.0 g, 423 mmol), tetrahydrofuran (80.0 mL), methanol (80.0 mL), and urea hydrogen peroxide addition compound (65.0 g, 691 mmol, Aldrich). The resulting white slurry was stirred overnight at 60° C. After cooling to ambient temperature, MnO₂ (0.56 g, 6.4 mmol) was added, and the mixture was stirred at this temperature for 4 h. The solids were removed by filtration, and the filter cake was washed with methanol. The combined filtrates were concentrated in vacuo. The residue was dissolved in water (100 mL) and extracted with a CHCl₃/i-PrOH mixture (3/1, v/v, 5×100 mL). The combined organic portions were dried over MgSO₄ and conc. in vacuo. After triturating the residue with CH₂Cl₂ and EtOAc, the white solid was collected by filtration. This material was the title compound. A second crop of desired product was obtained by flash column chromatography (0-5% MeOH in EtOAc) from the concentrated filtrate.

Example 100 (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol

To a stirred solution of (1R,2S,4R,5S)-bicyclo[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10° C. (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and 1-(bromomethyl)benzene (1.07 mL, 8.97 mmol). After stirring at 10° C. for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.

Example 101 (1R,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-one

Silica gel 60 (particle size, 0.040-0.063 mm, CAS # 63231-67-4, from EMD Chemical Inc. 9.0 g) was added to a solution of (1R,2S,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-ol (2.79 g, 12.8 mmol) in anhydrous dichloromethane (60.0 ml). The mixture was cooled to 0° C., and pyridinium chlorochromate (4.40 g, 20.4 mmol) was added. The reaction mixture was warmed to ambient temperature and stirred at this temperature for 5 h. After this time, the mixture was diluted with dichloromethane (60 mL) and then filtered through a pad of Celite. The solvent was removed in vacuo, and the residue was purified by flash column chromatography (0 to 25% of ethyl acetate in hexanes) to give the title compound as a colorless oil.

Example 102 (1R,4R,5S)-5-(Benzyloxy)-2,2 difluorobicyclo-[2.2.1]heptane

Deoxo-Fluor (50% in THF, 17.7 g, 40.0 mmol) was added to (1R,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-one (2.45 g, 11.3 mmol) in a 250 mL round-bottom flask. The mixture was heated to 85° C. (oil bath temperature) and stirred at this temperature under nitrogen for 16.5 h. After cooling to ambient temperature, the mixture was diluted with ethyl acetate, then poured into sat'd NaHCO₃ in ice. The organic portion was separated, washed with brine, dried over MgSO₄, filtered, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 5% of ethyl acetate in hexanes) to give the title compound as a colorless oil.

Example 103 (1R,2S,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-ol

Palladium (10 wt. % on activated carbon, 0.28 g) was added to a solution of (1R,4R,5S)-5-(benzyloxy)-2,2-difluorobicyclo[2.2.1]-heptane (1.43 g, 6.0 mmol) in methanol (15 mL), and the mixture was placed under a balloon full of hydrogen.After stirring at ambient temperature for 4 h, the mixture was filtered through a pad of Celite, and the filtrate was concentrated in vacuo. The residue was adsorbed onto a small pad of silica gel, and eluted with 20% of ethyl acetate in hexanes. The solvents were removed in vacuo to give the title compound as a white solid.

Example 104 (1R,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-one

Silica gel 60 (particle size, 0.040-0.063 mm, CAS # 63231-67-4, from EMD Chemical Inc. 4.0 g) was added to a solution of (1R,2S,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-ol (0.800 g, 5.40 mmol) in anhydrous dichloromethane (20.0 ml). The mixture was cooled to 0° C., and pyridinium chlorochromate (1.86 g, 8.64 mmol) was added. The reaction mixture was warmed to ambient temperature and stirred at this temperature overnight. After this time, the mixture was diluted with dichloromethane (30 mL) and then filtered through a pad of silica gel. Removal of the solvents gave the title compound as a white solid.

Example 105 (1R,2R,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-ol

To a solution of (1R,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-one (0.540 g, 3.7 mmol) in anhydrous tetrahydrofuran (8.00 mL) at −78° C. under nitrogen was added drop-wise L-Selectride (1.0 M solution in tetrahydrofuran, 7.40 mL). After stirring at −78° C. for 3 h, 30% H₂O₂ (6.0 mL) and 10% NaOH (aq., 10.0 mL) were added. The mixture was warmed to r.t. and then stirred at 65° C. for 10 h. After cooling to ambient temperature, the mixture was extracted with EtOAc (50 mL×2). The combined organic portions were washed with brine, and conc. in vacuo. Flash column chromatography (0 to 30% of ethyl acetate in hexanes) gave the title compound as a white solid.

Example 106 2-((1R,2S,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-yl)isoindoline-1,3-dione

A solution of diethyl azodicarboxylate (0.56 mL, 3.6 mmol) in anhydrous THF (3.0 mL) was added drop-wise to a mixture of (1R,2R,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-ol (0.44 g, 3.0 mmol), phthalimide (0.50 g, 3.4 mmol), and triphenyl phosphine (0.78 mL, 3.4 mmol) in anhydrous tetrahydrofuran (15.0 mL) at r.t. under nitrogen. After stirring at ambient temperature for 66 h, the solvents were removed in vacuo. The residue was partitioned between ethyl acetate and water, and the organic portion was separated, washed with brine, and conc. in vacuo. Flash column chromatography (0 to 35% of ethyl acetate in hexanes) gave the title compound as an off-white solid.

Example 107 (1R,2S,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-amine hydrochloride

To a suspension of 2-((1R,2S,4R)-5,5-difluorobicyclo[2.2.1]-heptan-2-yl)isoindoline-1,3-dione (0.58 g, 2.09 mmol) in ethanol (anhydrous, 30 mL) was added hydrazine (0.10 mL, 3.14 mmol). After refluxing this mixture under nitrogen for 5 h, it was cooled in an ice bath, and hydrochloric acid (37%, 0.50 mL) was added. After stirring at 60° C. for 1.5 h, the mixture was cooled to ambient temperature. After the white solid was removed by filtration, the filter cake was washed with methanol, and the filtrate was conc. in vacuo. The resulting residue was diluted in ˜50 mL of water, filtered, and the filtrate was washed with diethyl ether (30 mL×3). The filtrate was then treated with sodium carbonate monohydrate to saturation, and the aqueous layer was extracted with diethyl ether (50 mL×3). These organic layers were combined, dried over potassium carbonate (solid), and filtered. The solution was treated with hydrochloric acid (1M aqueous, 4 mL), stirred for 5 min, and then concentrated in vacuo to give the title compound as a white solid.

Example 108 1-Benzoyl-3-((1R,2S,4R)-5,5-difluorobicyclo-[2.2.1]heptan-2-yl)thiourea

Benzoyl isothiocyanate (0.32 mL, 2.34 mmol) was added to the mixture of (1R,2S,4R)-5,5-difluorobicycle[2.2.1]heptan-2-amine hydrochloride (0.33 g, 1.80 mmol) and triethylamine (0.38 mL, 2.70 mmol) in anhydrous chloroform (25.0 mL) atambient temperature under nitrogen. After stirring overnight, the reaction mixture was concentrated in vacuo. Water (50 mL) was added to the residue, and it was extracted with diethyl ether (2×50 mL). The organic portions were combined, washed with brine, and conc. in vacuo to give a light yellowish oil as the title compound that was used in the following reaction without purification. Mass Spec m/z: 311.1 (M+H)⁺.

Example 109 1-((1R,2S,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-yl)thiourea

A mixture of 1-benzoyl-3-((1R,2S,4R)-5,5-difluorobicyclo-[2.2.1]heptan-2-yl)thiourea (˜1.80 mmol) and potassium carbonate (1.49 g, 10.8 mmol) in methanol (5.0 mL), water (2.5 mL), and tetrahydrofuran (2.5 mL) was stirred at ambient temperature for 2 h. The reaction mixture was concentrated in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was washed with brine, conc. in vacuo, and purified by flash column chromatography (0 to 65% of ethyl acetate in hexanes) to give the title compound as a white solid. MS m/z: 207.0 (M+H)⁺.

Example 110 2-(2-Chlorophenyl)-2-methylpropanenitrile

Method R

A 500 mL round-bottomed flask was charged with 2-(2-chlorophenyl)acetonitrile (6.82 g, 0.045 mol) and 30 mL of THF. This solution was cooled to −40° C., and KHMDS (0.5 M in toluene, 200 mL, 0.100 mol) was added at such a rate that the internal temperature did not rise above −40° C. This solution was allowed to stir between −40 to −50° C. for an additional 1 h. After that time, MeI (14.2 g, 6.25 mL, 0.100 mol) was added and the solution was warmed to room temperature (a thick solid formed). The reaction was stirred for 1 h at room temperature then quenched by the addition of saturated aqueous NaHCO₃. The layers were separated, and the aqueous phase was extracted with CH₂Cl₂. The combined organic extracts were dried and concentrated in vacuo to give an oil that was purified by column chromatography (SiO₂, 100% hexanes to 90% hexanes/ethyl acetate) to provide 2-(2-chlorophenyl)-2-methylpropanenitrile as a colorless oil.

Example 111 2-(2-Chlorophenyl)propan-2-amine

2-(2-Chlorophenyl)-2-methylpropanenitrile (5.0 g, 0.028 mol) along with 50 mL of EtOH was added into a 250 mL round-bottomed flask. To this was added 50 mL of saturated aqueous K₂CO₃. This mixture was cooled to 0° C. then 85 mL of 30% aqueous H₂O₂ was slowly added. The reaction mixture was allowed to warm to room temperature, and then it was stirred at that temperature for 12 h. The mixture was extracted with CH₂Cl₂ (3×150 mL), and the combined organic extracts were dried over MgSO₄, filtered, and concentrated in vacuo to give a viscous oil. To this oil was added 40 mL of CH₃CN, 40 mL H₂O, and 13.2 g (0.031 mol) of PhI(O₂CCF₃)₂. This mixture was stirred at r.t. for 12 h, diluted with 300 mL of H₂O, and then stirred for an additional 4 h at room temperature. The aqueous phase was extracted using MTBE (1×200 mL) follow by diethyl ether (2×100 mL). The aqueous layer was basified with 1N NaOH (pH=13) and then extracted with CH₂Cl₂ (3×100 mL). The organic extracts were dried and concentrated in vacuo to give the desired product as a colorless oil that was used in subsequent steps without further purification.

Example 112 2-Bromobicyclo[2.2.1]heptane-1-carboxylic acid

Method S

To a 50 mL round-bottomed flask was added (1S,4R)-bicyclo[2.2.1]heptane-2-carboxylic acid (9.84 g, 70 mmol) and bromine (4.10 ml, 80 mmol). The suspension was stirred at room temperature until dissolution. Trichlorophosphine (0.30 ml, 3.4 mmol) was then added slowly and drop wise (significant exotherm observed). A reflux condenser was fitted to the flask with a nitrogen gas inlet and gas outlet (Tygon tubing) running into a scrubber solution of sodium sulfite (1 M, 200 mL). After the addition was complete, the reaction mixture was heated in a silicone oil bath at 80° C. for 4 h. After this time, the reaction was cooled to 10° C. and phosphorus-trichloride (4.23 ml, 48.3 mmol) was added drop-wise. The reaction was then heated to 80° C. During this time the color intensity of the reaction decreased, and after 8 h, the reaction mixture appeared dark orange. The reaction was then cooled to room temperature and diluted with ether (1 L). The ethereal solution was transferred to a separation funnel and washed with 1M sodium sulfite (2 (500 mL), water (1 (500 mL), and brine (1 (500 mL). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to afford an oil. Ice cold pentane (50 mL) was then added to the crude product, and the mixture was stirred vigorously. After 20 min, a fine white precipitate formed, which was filtered and washed with pentane (20 mL) and then air dried under a gentle vacuum to afford (4S)-2-bromobicyclo[2.2.1]heptane-1-carboxylic acid (100.2 g, 457 mmol) as a white solid material.

Example 113 Bicyclo[2.2.1]heptane-1-carboxylic acid

A 2-L reactor equipped with an overhead mechanical stirrer, condenser, nitrogen gas inlet port, temperature probe and reagent charging port, was placed under an atmosphere of nitrogen. The reactor was charged with zinc powder (<10 micron) (298 g, 4560 mmol) and acetic acid (500 mL). While vigorously stirring the heterogeneous mixture, (4S)-2-bromobicyclo[2.2.1]heptane-1-carboxylic acid (100 g, 456 mmol) was then added. A second portion of acetic acid (500 mL) was then used to rinse the walls of the reactor. The reaction mixture was brought to a gentle reflux (ca. 30 min) and then held at this temperature for 5 h. The cooled (room temperature) reaction mixture was passed through a pad of Celite, which was washed with acetic acid (1 (300 mL) and ethyl acetate (1 (500 mL). The filtrate was concentrated, water (300 mL) was added, and then the mixture was stirred vigorously to induce precipitation. The precipitate was collected by filtration, washed with water, and dried under vacuum at 35° C. overnight. Pentane (50 mL) was then added, and the mixture was stirred vigorously for 20 min during which time a fine white precipitate formed. The resulting precipitate was filtered, washed with pentane (20 mL), and air dried to afford bicyclo[2.2.1]heptane-1-carboxylic acid (52 g) as a white solid.

Example 114 tert-Butyl bicyclo[2.2.1]heptan-1-ylcarbamate

A 100 mL round-bottomed flask equipped with a condenser and nitrogen inlet was charged with bicyclo[2.2.1]heptane-1-carboxylic acid (2.00 g, 14.3 mmol), toluene (35 mL), triethylamine (2.18 ml, 15.7 mmol) and diphenylphosphoryl azide (3.38 ml, 15.7 mmol) at room temperature under an atmosphere of nitrogen. Thereaction mixture was stirred at room temperature for 1 h before being heated to 50° C. for 3 h. Gas evolved from the reaction mixture for approximately 2-3 h. After 3 h at 50° C., the temperature of the reaction mixture was increased to 70° C. and stirring continued for another 2 h until no further gas evolution occurred. The reaction mixture was then cooled and then concentrated in vacuo. The resulting oil was dissolved in anhydrous t-BuOH (10 mL, 99.9% anhydrous packed under argon; Alfa Aesar), placed under and atmosphere of nitrogen, and refluxed in a 90 (C bath for 14 h. After this time, the reaction mixture was cooled and concentrated under reduced pressure to afford an off-white solid which was then dissolved in ether (50 mL), washed with water (20 mL), 1M NaOH (20 mL), water (20 mL) and brine (20 mL). After being dried over MgSO4, the mixture was filtered and concentrated in vacuo to afford 2.2 g of an off-white solid. Pentane (20 mL) was added, and solution was stirred vigorously until the majority of the material dissolved. The light orange colored precipitate that did not dissolve was removed through a fine grade sintered glass filter funnel. The mother liquor was concentrated to afford the title compound (2.2 g) as an off white solid.

Example 115 1-(Bicyclo[2.2.1]heptan-1-yl)thiourea

A 100 mL RBF was purged with nitrogen gas before being charged with tert-butyl bicyclo[2.2.1]heptan-1-ylcarbamate (6.60 g, 31.0 mmol) and dichloromethane (66 mL). The solution was cooled in a 0° C. a bath, and then trifluoroacetic acid (12 mL, 18 g, 156 mL) was added. The cooling bath was removed, and the reaction mixture was allowed to warm to room temperature during which time a gas evolved from the reaction mixture. After 3 h at room temperature the reaction mixture was concentrated in vacuo to afford a viscous oil. This material was dissolved in dichloromethane (82 mL), and triethylamine (13.0 mL, 94 mmol) and benzoyl isothiocyanate (4.6 mL, 34 mmol) were added. After stirring at room temperature under an atmosphere of nitrogen for 14 h, the reaction mixture was concentrated in vacuo, and the resulting residue was dissolved in MeOH/THF/H₂O (2:1:1, ca. 0.3 M). Potassium carbonate (22 g, 156 mmol) was added, and the biphasic solution was vigorously stirred for 3 h. The organic solvents were removed under reduced pressure during which time a yellow precipitate formed. The precipitate was filtered, washed with water (30 ml) and cold (−20° C.) diethyl ether to provide a white precipitate. This material was allowed to air dry for 10 min and then dried under high vacuum at room temperature for ca. 18 h to afford the title compound (3.8 g) as a fine white powder.

Example 116 4-(2-(4-Methyl-3-nitrophenoxy)ethyl)morpholine

Method T

A mixture of 4-methyl-3-nitrophenol (1.53 g, 10 mmol.), 4-(2-chloroethyl)morpholine (2.79 g, 15 mmol), Cs₂CO₃ (9.78 g, 30 mmol) and NaI (145 mg, 1 mmol) in DMF (15 mL) was stirred for 3 h at 80° C. The reaction mixture was then cooled to room temperature, diluted with water, and extracted with EtOAc. The organic layer was dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1:0.05 CH₂Cl₂/EtOAc/MeOH) to give the title compound as an oil.

Example 117 2-Methyl-5-(2-morpholinoethoxy)benzenamine

To the mixture of 4-(2-(4-methyl-3-nitrophenoxy)ethyl)morpholine (532 mg, 2 mmol) in MeOH (50 mL) was added 10% Pd/C (250 mg). The mixture was stirred under an atmosphere of H₂ (balloon) overnight. The contents of the reaction mixture were then filtered and concentrated in vacuo to give the title product, which was used without further purification.

Example 118 1-(2-Chlorophenyl)cyclopropanamine

Method U

This compound was prepared using the method described by Bertus and Szymoniak; J. Org. Chem. 2003, 68, 7133.

Example 119 tert-Butyl 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-ylcarbamate

Method V

To a flame-dried 100 mL round-bottomed flask equipped with magnetic stirring and argon inlet/outlet was added 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octane-1-carboxylic acid (200 mg, 649 μmol, prepared by the method described in US Patent Application: 2004/0133011 and 5 mL of toluene. Triethylamine (0.10 mL, 713 μmol) was added followed by diphenylphosphoryl azide (0.2 mL, 713 μmol), and the reaction mixture warmed in a 50° C. oil bath for 30 min, then to 70° C. for 5 h. tert-Butanol (5 mL, 53 mmol) was then added, and the reaction mixture continued to stir in the 70° C. bath. After 20 h, copper (I) chloride (10 mg, 101 μmol) was added, and the reaction continued to stir for ca 1.5 d at 70° C. The reaction was removed from the oil bath and then poured thru a 1 cm pad of Celite. The Celite pad was washed with CH₂Cl₂, and the filtrate was concentrated in vacuo. CH₂Cl₂ (50 mL) was added to the filtrate, and the organic layer was washed with 1M NaOH (2×), sat'd NH₄Cl, sat'd NaHCO₃, and brine. The organic layer was then dried over MgSO₄, filtered and concentrated in vacuo to give tert-butyl 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-ylcarbamate (mass=170 mg). The crude reaction product was taken onto the next step without further purification.

Example 120 4-(4-(Methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-amine

To a 100 mL round-bottomed flask equipped with magnetic stirring was added tert-butyl 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-ylcarbamate (170 mg, 448 μmol), 2 mL of CH₂Cl₂, ca. 5 drops of water, and trifluoroacetic acid (2 mL, 27 mmol). The reaction mixture was stirred at ambient temperature for 3.5 h, after which time the mixture was concentrated in vacuo. NaOH (ca. 50 mL of a 1M aq. solution) was added to the mixture, and the aqueous layer was extracted with CH₂Cl₂ (3×15 mL). The organic layers were combined, dried over K₂CO₃, filtered, and concentrated in vacuo to give 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-amine (mass=120 mg, Mass Spec. m/z+ion=280.2) The crude reaction product was taken onto the next step without further purification.

Example 121 1-Benzoyl-3-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-yl)thiourea

To a 100 mL round-bottomed flask equipped with magnetic stirring was added 4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-amine (120 mg, 429 μmol) in 2 mL of CH₂Cl₂, and benzoyl isothiocyanate (63.6 μl, 472 μmol). The reaction was stirred at ambient temperature for ca. 26 h, and then it was concentrated in vacuo to give 1-benzoyl-3-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-yl)thiourea (mass=185 mg, Mass spec. m/z+ion=443.2). The crude reaction product was taken onto the next step without further purification.

Example 122 1-(4-(4-(Methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-yl)thiourea

To a 100 mL round-bottomed flask equipped with magnetic stirring was added a solution of 1-benzoyl-3-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-yl)thiourea (185 mg, 418 μmol) suspended in THF (1.5 mL) and methanol (3 mL). A solution of potassium carbonate (289 mg, 2090 μmol) in 1.5 mL of water was added, and the reaction mixture was stirred at ambient temperature. After 3.5 h, 3 mL more of THF was added. Then after 22.5 h, the lower boiling solvents of the reaction mixture were removed in vacuo. Water was added, and the aqueous layer was extracted with EtOAc (1×10 mL), CH₂Cl₂ (3×10 mL), and EtOAc (1×20 mL). The aqueous layer was the saturated with solid NaCl, and it was extracted with THF (3×10 mL). All organic layers were combined along with 30 mL more THF and dried over K₂CO₃, filtered, and concentrated in vacuo. The residue was absorbed onto silica gel and purified on a 40 g silica gel column using 1:2 hexanes-EtOAc+2% MeOH as the eluant followed by 1:2 hexanes-EtOAc+4.5% MeOH. Purified 1-(4-(4-(methylsulfonyl)phenyl)bicyclo[2.2.2]octan-1-yl)thiourea was isolated from the chromatography (43 mg, white solid, Mass spec. m/z+ion=339.2).

Example 123 Bicyclo[2.2.1]heptane-2-carboxamide

Method W

A round-bottomed flask was charged with 450 g exo-2-norbornyl carboxylic acid (3200 mmol) in 100 mL of CH₂Cl₂. To the solution was added 0.23 mL of DMF (3.21 mmol) followed by the drop-wise addition of 325 mL of oxalyl chloride (3700 mmol). The reaction was stirred for 1 h at ambient temperature then warmed to 45° C. for an additional 30 min. The reaction was allowed to cool to ambient temperature and 2.5 L of 28% NH₄OH was slowly added. The reaction was stirred for 1 h at ambient temperature. The desired product was isolated by filtration.

Example 124 1-Benzoyl-3-(bicyclo[2.2.1]heptan-2-ylmethyl)thiourea

A dry 500 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N₂ was charged with 3.96 g (28.5 mmol) of bicyclo[2.2.1]heptane-2-carboxamide in 30 mL of anhydrous THF. The mixture was cooled to 0° C. and 57 mL (57 mmol) of lithium aluminum hydride (1.0 M in THF) were added via syringe. The reaction was stirred for 10 min. at 0° C. then allowed to warm to ambient temperature and stirred an additional 15 h. The reaction solution was then cooled to 0° C., and 2.2 mL of H₂O were added drop-wise followed by the addition of 2.2 mL of 15% aq. NaOH. Water (6.6 mL) was then added and the reaction was allowed to stir for 0.5 h at ambient temperature. The solids were removed by filtration through a Celite pad. Trifluoroacetic acid (2.6 mL) was then added to the filtrate, and the mixture stirred for 1 h at ambient temperature. The solvent was removed in vacuo providing amine salt as a white solid.

A dry 150 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N₂ was charged with 5.46 g (22.8 mmol) of amine salt in 50 mL of CH₂Cl₂. To the solution was added 6.5 mL (46.6 mmol) of triethylamine followed by the drop-wise addition of 3.05 mL (22.7 mmol) of benzoyl isothiocyanate. After stirring the reaction mixture for 1.3 h at ambient temperature, the organic layer was washed with H₂O (2×25 mL), 1M KOH (2×25 mL), 1M HCl (2×25 mL), and brine. The organic phase was dried over MgSO₄, filtered, and concentrated in vacuo to provide the desired N-acylthiourea. MS (ESI, pos. ion) m/z: 289.2 (M+H).

Example 125 1-(Bicyclo[2.2.1]heptan-2-ylmethyl)thiourea

A 250 mL round-bottomed flask equipped with a magnetic stir bar was charged with 6.17 g (22.4 mmol) of 1-benzoyl-3-(bicyclo[2.2.1]heptan-2-ylmethyl)thiourea in 30 mL of MeOH. KOH was added (2.55 g, 45.4 mmol) and the reaction was stirred at ambient temperature for 4 h. Water (150 mL) was then added to the reaction mixture, and the solid was removed by filtration. The flask and filter cake were rinsed with 40 mL of H₂O. The collected solid was then suspended in 15 mL of MTBE, and the solid was collected by filtration providing the desired thiourea. MS (ESI, pos. ion) m/z: 185.2 (M+H).

Synthesis of Final Products. (procedures: Method-X, Method-Y, Method-Z, Method-AA, Method-BB, Method-CC, Method-DD, Method-EE, Method-FF, Method-GG, Method-II, Method-JJ, Method-KK, Method-LL Method-MM, Method-NN, Method-OO, Method-PP).

Example 126 6-(Cycloheptylamino)-5-thia-7-azaspiro[3.4]oct-6-en-8-one

Method X

A mixture of 1-cycloheptylthiourea (0.255 g, 1.48 mmol) and ethyl 1-bromocyclobutanecarboxylate (0.25 mL, 1.48 mmol, Aldrich) in N,N-diisopropylethylamine (0.5 mL) and ethanol (1.0 mL) was heated in a sealed tube in a microwave oven (Emrys Optimizer from Personal Chemistry) at 155° C. for 2 h, then at 170° C. for 1.5 h. After removing the low-boiling solvents in vacuo, the residue was partitioned between EtOAc and water. The organic portion was separated, washed with brine, and conc. in vacuo. The residue was purified by flash column chromatography (0 to 35% of EtOAc in hexanes) to give the title compound as a tan solid. MS m/z: 253.2 (M+H)⁺

Example 127 Ethyl 4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazole-5-carboxylate

Method X

To a stirred solution of 2-(trifluoromethyl)phenylthiourea (Menai Organics, 2.36 g, 10.7 mmol), Hunig's base (Aldrich, 1.9 mL, 10.7 mmol) in EtOH (10 mL) was added diethyl bromomalonate (2.0 mL, 10.7 mmol). After 1.5 h at room temperature, the reaction mixture was diluted with EtOAc, washed with saturated NaHCO₃ and brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 333 (M+1).

Example 128 (5R)-(±)-endo-2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

Method Y

To a stirred solution of (±)-endo-1-(bicyclo[2.2.1]heptan-2-yl)thiourea (314 mg, 1.84 mmol) and (S)-2-bromo-3-methylbutanoic acid (334 mg, 1.84 mmol) in anhydrous ethanol (10 mL) under nitrogen, was added sodium acetate (182 mg, 2.21 mmol, 1.2 equ.) at room temperature. After refluxing the reaction mixture for 3 h, the solvent was evaporated in vacuo, and the residue was taken up in ethyl acetate (20 mL). The organic layer was washed with water (20 mL) followed by brine (20 mL), then dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO₂ 4:1 hexane/acetone) to afford the title compound (90 mg). MS (ESI, pos. ion) m/z: 253.1 (M+H).

Example 129 (S)-2-((rel-1R,2R,4S)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

Method Z

To a solution of (R)-2-bromo-3-methylbutanoyl isothiocyanate (734 mg, 3.30 mmol) in CH₂Cl₂ at 0° C. was added drop-wise exo-2-aminonorbornane (0.4 mL, 3.37 mmol). The mixture was allowed to stir for 30 min at 0° C. Triethylamine (0.47 mL, 3.38 mmol, 1.02 equiv) was then added, and the mixture allowed to warm to room temperature and stirred overnight. The mixture was concentrated and the resulting oil triturated with THF (26 mL), filtered, and concentrated in vacuo. Flash chromatography (gradient of hexanes:acetone gradient—automated, hexanes:acetone 4:1—manual) furnished the title compound as a sticky white solid. Material was foamed by dissolution in CH₂Cl₂ followed by re-concentration.

Example 130 5-Isopropyl-5-methyl-2-(pyridin-2-ylmethylamino)thiazol-4(5H)-one

Method Z

Pyridin-2-ylmethanamine (0.22 mL, 2.1 mmol) was added to 2-bromo-2,3-dimethylbutanoyl isothiocyanate (240 mg, 1.1 mmol) at room temperature. The reaction was exothermic, and was stirred at room temperature for 15 min. CH₂Cl₂ (2 ml) was added, and the resulting precipitate was removed by filtration. The CH₂Cl₂ solution was concentrated, and the mixture was purified by silica gel column (gradient 1% (10% NH₃ in MeOH) to 30% (10% NH₃ in MeOH) in CH₂Cl₂) to give the title compound as an off-white solid (123 mg). Mass Spec.=m/z+ion 264.1 (M+H)

Example 131 5-Cyclopentyl-5-fluoro-2-(2-fluorophenylamino)thiazol-4(5H)-one

Method BB

A dry 100 mL round-bottomed flask was charged with 5-cyclopentyl-2-(2-fluorophenylamino)thiazol-4(5H)-one (0.200 g, 0.717 mmol) and 6.0 mL of THF. This solution was cooled to −78° C., and LDA (2.0 M in THF/heptane/ethyl benzene, 1.43 mL, 2.86 mmol) was added. The resulting brown solution was allowed to stir at that temperature for 1 h, then TMSCl (0.623 g, 0.725 mL, 5.74 mmol) was added. The solution was warmed to room temperature and allowed to stir for an additional 1 h. The solution was concentrated in vacuo to remove the volatiles and then redissolved in 10 mL of CH₃CN. Selectfluor® (0.508 g, 1.43 mmol) was added at room temperature, and the resulting solution was stirred for 2 h. The reaction was quenched with saturated aqueous NaHCO₃, and the resulting mixture was thoroughly extracted with CH₂Cl₂. This combined organic extracts were dried and concentrated in vacuo to give an oil which was purified by column chromatography (100% to 70% hexanes/30% ethyl acetate) to give the title compound as a colorless oil. Mass Spec (M+H)⁺; 297.1.

Example 132 2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(trifluoromethyl)thiazol-4(5H)-one

Method CC

A dry 100 mL round-bottomed flask equipped with a magnetic stir bar under an atmosphere of N₂ was charged with 528 mg (2.35 mmol) of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one in 5 mL of anhydrous THF. The reaction was cooled to −20° C. and 5.0 mL (5.0 mmol) of NaHMDS (1.0M in THF) were added drop-wise via syringe. The resulting reaction mixture was stirred at −20° C. for 30 min then 0.86 mL (6.78 mmol) of TMSCl was added drop-wise via syringe. The reaction mixture was held at −20° C. for 15 min, and then the mixture was allowed to warm to ambient temperature. After stirring the reaction mixture for an additional 1 h, the mixture was concentrated in vacuo. The reaction flask was again equipped with a magnetic stir bar and placed under an N₂ atmosphere. Anhydrous CH₃CN was added, and 978 mg (2.58 mmol) of S-(trifluoromethyl)dibenzothiophenium-3-sulfonate C₂H₅OH was added to the reaction mixture in one portion, and the resulting suspension was stirred at ambient temperature for 19 h. The solids were then removed by filtration through a Celite pad, and the reaction flask and pad were rinsed with CH₂Cl₂. The organic layer was washed with 20 mL of 1:1 H₂O/sat'd NH₄Cl, and the aqueous layer was extracted with an additional portion of CH₂Cl₂. The combined organic layers were washed with brine, dried over MgSO₄, filtered, and concentrated in vacuo. Flash chromatography (SiO₂, CH₂Cl₂ to 5% MeOH/CH₂Cl₂) provided the desired compound. MS (ESI, pos. ion) m/z: 293.1 (M+H).

Example 133 Ethyl 5-(3-tert-butoxy-3-oxopropyl)-4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazole-5-carboxylate

Method DD

The above compounds were prepared according to the procedure reported in the literature: see S. Muthusamy Synth. Commun. 2002, 32, 3247. To a stirred solution of ethyl 4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazole-5-carboxylate (1.1 g, 3.3 mol), tert-butyl acrylate (Aldrich, 2.5 mL, 16.5 mmol) in EtOH (10 mL) was added DBU (Aldrich, 0.25 mL, 1.6 mmol). The mixture was stirred at r.t. overnight and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 461 (M+1).

Example 134 tert-Butyl 3-(4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazol-5-yl)propanoate

To a mixture of ethyl 5-(3-tert-butoxy-3-oxopropyl)-4-oxo-2-(2-(trifluoromethyl)phenylamino)-4,5-dihydrothiazole-5-carboxylate (88.7 mg, 0.19 mmol), THF (1 mL), MeOH (0.3 mL), and water (0.3 mL) was added LiOH.H₂O (Aldrich, 20 mg, 0.47 mmol) at room temperature. After 3 h, 1N HCl (0.7 mL) was added to the reaction mixture at 0° C. The mixture was extracted with EtOAc, and the organic phase was dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude material was purified by silica gel chromatography. MS: 389 (M+1).

Example 135 2-((1S,2S,4R)-Bicyclo[2.2.1]hept-2-ylamino)-8-oxa-1-thia-3-azaspiro[4.5]dec-2-en-4-one

Method EE

To the mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (840 mg, 4.0 mmol) in THF (5.0 mL) was added LDA (2.0 M, 20 mL) at −78° C. The resulting mixture was stirred for 10 min at −78° C., and then 1-bromo-2-(2-bromoethoxy)ethane (3.71 g, 16 mmol) was added. The mixture was allowed to warm to room temperature and then stirred overnight. A sat'd solution of NaH₂PO₄ was added, and it was extracted with EtOAc. The organic layer was washed with sat'd NH₄Cl, dried over MgSO₄, filtered, and concentrated in vacuo. The crude residue was purified through flash chromatography (4:1:0.05; CH₂Cl₂/EtOAc/MeOH) to give the title compound as off-white solid. MS (ES⁺): 281 (M+H)⁺.

Example 136 2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxypropan-2-yl)-5-methylthiazol-4(5H)-one

Method FF

To a solution of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one (1.10 g, 5.0 mmol) in THF (5 ml) at −78° C. was added LDA (2.0 M, 10 ml). After 5 min, acetone was added, and the reaction mixture was stirred for 1 h at −78° C. The resulting reaction mixture was poured into a sat'd NaH₂PO₄, and extracted with EtOAc. The organic layer was dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as a white solid. MS (ES⁺): 283 (M+H)⁺. The diastereomers were separated using standard HPLC methods described within this text.

Example 137 2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-fluoropropan-2-yl)-5-methylthiazol-4(5H)-one

Method GG

To the solution of DAST (527 mg, 3.3 mmol) in CH₂Cl₂ (2 ml) at −78° C. was added a solution of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxypropan-2-yl)-5-methylthiazol-4(5H)-one in CH₂Cl₂ (8 ml) over 10 min. After the addition, the cold bath was removed and the temperature was allowed to warm up to 0° C., and then quenched with sat'd NaHCO₃. The mixture was extracted with CH₂Cl₂, dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as white solid. MS (ES⁺): 285 (M+H)⁺. The diastereomers were separated using standard HPLC methods described within this text.

Example 138 5-Isopropyl-5-methoxy-2-(tricyclo[3.3.1.1^(3,7)]decan-1-ylamino)-thiazol-4-one

Method II

A mixture of 5-(1-methylethyl)-2-(tricyclo[3.3.1.1^(3,7)]dec-1-ylamino)-1,3-thiazol-4(5H)-one (146 mg, 0.5 mmol) and NBS (107 mg, 0.6 mmol) in CCl₄ (60 mL) was stirred at reflux for 30 min. The resulting mixture was cooled to 0° C., andfiltered to remove the solid. The residue was then concentrated in vacuo and diluted with CH₂Cl₂ (20 mL). To this mixture was added MeOH (200 μL) and DIEA (200 μL). The mixture was stirred for 30 min, then was concentrated in vacuo and purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as white solid. MS (ES⁺): 323 (M+H)⁺.

Example 139 2-(2-(1-Adamantylamino)-4-oxo-4,5-dihydrothiazol-5-yl)acetaldehyde

Method JJ

A suspension of 2-(1-adamantylamino)-5-(2-hydroxyethyl)thiazol-4(5H)-one (0.25 g, 0.85 mmol) in CH₂Cl₂ (10 mL) was added to Dess-Martin periodinane (0.56 g, 1.28 mmol, Aldrich) in CH₂Cl₂(10 mL). After stirring at ambient temperature for 1 h, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and saturated aqueous sodium thiosulfate and aqueous sodium bicarbonate. The organic portion was separated, washed with brine, and conc. in vacuo to give the title compound as a light yellowish solid. MS m/z: 293.6 (M+H)⁺.

Example 140 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)thiazol-4(5H)-one

Method KK

1-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-yl)thiourea (887 mg, 5.25 mmol), 3-bromo-dihydrofuran-2(3H)-one (1.65 g, 5 mmol), EtOH (10 mL) and DIEA (5.0 mL) were placed in a microwave reaction vessel. The mixture was placed in a microwavesynthesizer and was irradiated at 150° C. for 30 min. The resulting mixture was poured into water and extracted with EtOAc and dried over MgSO₄. After being filtered and concentrated in vacuo, the title compound was obtained a brown solid. MS (ES⁺): 255 (M+H)⁺.

Example 141 2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one

The mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)thiazol-4(5H)-one (3.2 g, 12.6 mmol) and p-toulenesulfonic acid (500 mg) in 3,4-dihydro-2H-pyran (10 mL) was stirred for 2 h at room temperature. The resulting mixture was diluted with CH₂Cl₂ (100 mL), then washed with sat'd NaH₂PO₄, and dried over MgSO₄. After being filtered and concentrated in vacuo, the crude residue was purified by flash chromatography (3:2; Hexane:EtOAc) to give the title compound as an oil. MS (ES⁺): 339 (M+H)⁺.

Example 142 2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-methylallyl)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one

To the mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one (1160 mg, 3.43 mmol) in THF (8.0 mL) cooled in a −78° C. bath was added LDA (2.0 M, 17.15 mL). The resulting mixture was stirred for 10 min at −78° C., and then 3-bromo-2-methylprop-1-ene (1.6 ml, 17.15 mmol) was added. After the reaction mixture was allowed to warm to room temperature and stirred ca. 18 h. Saturated NaH₂PO₄ was added, and the aqueous phase was extracted with EtOAc. The organic layer was washed with sat'd NH₄Cl, dried over MgSO₄, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as yellow oil. MS (ES⁺): 393 (M+H)⁺.

Example 143 2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)-5-(2-methylallyl)thiazol-4(5H)-one

The mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-methylallyl)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one (420 mg, 1.07 mmol) and p-toluenesulfonic acid (100 mg) in MeOH (5.0 mL) was stirred for 16 h at room temperature. The reaction mixture was then concentrated in vacuo, and sat'd NaH₂PO₄ was added. The mixture was then extracted with EtOAc, and the organic layer was washed with sat'd NH₄Cl, dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as solid. MS (ES⁺): 309 (M+H)⁺.

Example 144 2-((1S,2S,4R)-Bicyclo[2.2.1]hept-2-ylamino)-7,7-dimethyl-8-oxa-1-thia-3-azaspiro[4.5]dec-2-en-4-one

To a solution of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)-5-(2-methylallyl)thiazol-4(5H)-one (120 mg) in CH₂Cl₂ (3 mL) was added concentrated H₂SO₄ (200 uL). The resulting mixture was stirred for 16 h, then concentrated in vacuo. The residue was treated with sat'd NaH₂PO₄ and extracted with CH₂Cl₂. The organic layer was washed with sat'd NH₄Cl, dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as solid. MS (ES⁺): 309 (M+H)⁺. The diastereomers were separated using standard HPLC methods described within this text.

Example 145 2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(tert-butyldimethylsilyloxy)ethyl)thiazol-4(5H)-one

Method LL

The title compound was prepared according to the procedure described in the preparation of tert-butyl 4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carboxylate by using 2-(bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (1.00 g, 4.76 mmol), lithium diisopropylamide (Aldrich, 2.0 M in heptane/THF/ethylbenzene, 8.5 mL, 19.0 mmol), and (2-bromoethoxy)(tert-butyl)dimethylsilane (Aldrich, 6.83 g, 28.5 mmol). The title compound was obtained as an off-white solid (950 mg). MS (ESI, pos. ion) m/z: 369 (M+H).

Example 146 2-(Bicyclo[2.2.1]heptan-2-ylamino)-5,5-bis(2-(tert-butyldimethylsilyloxy)ethyl)thiazol-4(5H)-one

The title compound was prepared according to the procedure described in the preparation of tert-butyl 4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carboxylate by using 2-(bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(tert-butyldimethylsilyloxy)ethyl)thiazol-4(5H)-one (630 mg, 1.71 mmol), lithium diisopropylamide (Aldrich, 2.0 M in heptane/THF/ethylbenzene, 4.27 mL, 8.55 mmol), and (2-bromoethoxy)(tert-butyl)dimethylsilane (Aldrich, 2.46 g, 10.25 mmol). The title compound was obtained as a sticky orange solid (771 mg). MS (ESI, pos. ion) m/z: 413 (M-TBDMS+2H).

Example 147 2-(Bicyclo[2.2.1]heptan-2-ylamino)-5,5-bis(2-hydroxyethyl)thiazol-4(5H)-one

A mixture of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5,5-bis(2-(tert-butyldimethylsilyloxy)ethyl)thiazol-4(5H)-one (771 mg, 1.46 mmol) in 15 mL of a 1% HCl solution in ethanol was stirred at room temperature for 3 h. The reaction mixture was then concentrated in vacuo. Flash column chromatography (silica gel, 0-8% MeOH—CH₂Cl₂) afforded the title compound as a colorless thin film (390 mg). MS (ESI, pos. ion) m/z: 299 (M+H).

Example 148 Methanesulfonic acid 2-[2-(bicyclo[2.2.1]hept-2-ylamino)-5-(2-methanesulfonyloxy-ethyl)-4-oxo-4,5-dihydro-thiazol-5-yl]-ethyl ester

To a mixture of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5,5-bis(2-hydroxyethyl)thiazol-4(5H)-one (280 mg, 0.94 mmol) and diisopropylethylamine (Aldrich, 412 mg, 3.19 mmol) in CH₂Cl₂ (5 mL) was added methanesulfonyl chloride (344 mg, 3.00 mmol, 3.2 eq), and the reaction mixture was stirred at room temperature for 18 h. The reaction mixture was then concentrated in vacuo to providethe title compound which was used without further purification. MS (ESI, pos. ion) m/z: 455 (M+H).

Example 149 2-(Bicyclo[2.2.1]hept-2-ylamino)-8-cyclopentyl-1-thia-3,8-diaza-spiro[4.5]dec-2-en-4-one

A mixture of methanesulfonic acid 2-[2-(bicyclo[2.2.1]hept-2-ylamino)-5-(2-methanesulfonyloxy-ethyl)-4-oxo-4,5-dihydro-thiazol-5-yl]-ethyl ester (half of the crude product from above) and cyclopentylamine (799 mg, 9.38 mmol) in CH₂Cl₂ (1.5 mL) was stirred at room temperature for 4 d. Flash column chromatography (silica gel, 0-10% MeOH in CH₂Cl₂) afforded the title compound as an off-white solid (52 mg). MS (ESI, pos. ion) m/z: 348 (M+H).

Example 150 tert-Butyl 4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carboxylate

Method AA

To a solution of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one in anhydrous THF (30 mL) at −78° C. under N₂ was added lithium diisopropylamide (Aldrich, 2.0 M in heptane/THF/ethylbenzene, 9.2 mL, 18.4 mmol). After stirring the reaction mixture at −78° C. for 1 h, a solution of 4-bromomethyl-piperidine-1-carboxylic acid tert-butyl ester (Pharma Core, 5.12 g, 18.4 mmol, 4.0 eq) in anhydrous THF (10 mL) was added under N₂. The resulting reaction mixture was stirred at −78° C. for 4 h. The cooling bath was removed, and the reaction mixture was stirred at ambient temperature for ca. 18 h. Saturated NH₄Cl was then added, and the THF was removed in vacuo. The residue was extracted with EtOAc (3×180 mL), and the combined organic layers were washed with saturated NaCl, dried over Na₂SO₄, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, 0-60% EtOAc in hexane) afforded the title compound as an off-white solid (1.42 g). MS (ESI, neg. ion) m/z: 420 (M−H).

Example 151 2-((2S)-Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one

Method MM

A mixture of tert-butyl 4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carboxylate (1.42 g, 3.37 mmol, 1.0 eq) in 50 mL of a 4.7 M HCl solution in EtOAc was stirred at roomtemperature. After 4 h, the reaction mixture was concentrated in vacuo. Aqueous Na₂CO₃ (2.0 M, 20 mL) was then added, and water was removed in vacuo. The residue was then triturated with 10% MeOH—CH₂Cl₂ (6×100 mL), and the combined triturating solution were concentrated in vacuo. The crude product was dissolved in CH₂Cl₂, filtered, and concentrated in vacuo to afford the title compound as a light orange solid (1.08 g). MS (ESI, pos. ion) m/z: 322 (M+H).

Example 152 tert-Butyl 2-(3-(4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carbonyl)phenoxy)ethylcarbamate

A mixture of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (534 mg, 1.66 mmol), 4-[2-(Boc-amino)ethyloxy]-benzoic acid (NeoMPS, 701 mg, 2.49 mmol), EDCI (Aldrich, 637 mg, 3.32 mmol, 2.0 eq), HOBt (Aldrich, 45 mg, 0.332 mmol, 0.2 eq) and triethylamine (Aldrich, 336 mg, 3.32 mmol, 2.0 eq) in CH₂Cl₂ (10 mL) was stirred at room temperature for ca. 18 h. The reaction was quenched with saturated NaHCO₃ (100 mL), and the crude product was extracted with CH₂Cl₂ (3×100 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, filtered, and concentrated. Flash column chromatography (silica gel, 0-5% MeOH in CH₂Cl₂) afforded the title compound as a white solid (800 mg). MS (ESI, pos. ion) m/z: 585 (M+H).

Example 153 5-((1-Acetylpiperidin-4-yl)methyl)-2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one

A mixture of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (130 mg, 0.41 mmol), acetic anhydride (Aldrich, 83 mg, 0.81 mmol) and diisopropylethylamine (157 mg, 1.22 mmol) in CH₂Cl₂ (3 mL) was stirred at room temperature for ca. 18 h. Brine was then added, and the mixture was extracted with CH₂Cl₂ (4×60 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, 0-3.5% MeOH in CH₂Cl₂) afforded the title compound as a colorless thin film (116 mg). MS (ESI, pos. ion) m/z: 364 (M+H).

Example 154 2-((2S)-Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-((1-(methylsulfonyl)piperidin-4-yl)methyl)thiazol-4(5H)-one

To a solution of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (64 mg, 0.20 mmol) in CH₂Cl₂ (1.5 mL) was added methanesulfonyl chloride (Aldrich, 34 mg, 0.30 mmol) and triethylamine (60 mg, 0.60 mmol), and the reaction mixture was stirred at room temperature for ca. 18 h. Water (30 mL) was then added, and the crude product was extracted with CH₂Cl₂ (3×60 mL). The combined organic extracts were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, 0-3% MeOH in CH₂Cl₂) afforded the title compound as a white solid (34 mg). MS (ESI, pos. ion) m/z: 400 (M+H).

Example 155 2-((1S,2S,4R)-Bicyclo[2.2.1]heptan-2-ylamino)-5-(2-bromoethyl)thiazol-4(5H)-one

Method NN

To a solution of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (2.98 g, 14.2 mmol) in THF (15 ml) at −78° C. was added LDA (2.0 N, 28.4 ml). After 5 min, 1,2-dibromoethane (4.87 mL, 56.8 mmol) was added, and the reaction mixture was stirred for 3 h at −78° C. The resulting reaction mixture was poured into sat'd NaH₂PO₄ and extracted with EtOAc. The organic layer was dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as a white solid. MS (ES⁺): 317 (M+H)⁺.

Example 156 2-((1S,2S,4R)-Bicyclo[2.2.1]hept-2-ylamino)-6,6-dimethyl-7-oxa-1-thia-3-azaspiro[4.4]non-2-en-4-one and 5-((1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino)-4-thia-6-azaspiro[2.4]hept-5-en-7-one

To a solution of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-bromoethyl)thiazol-4(5H)-one (134 mg, 0.5 mmol) in THF (1 mL) at −78° C. was added LDA (2.0 N, 1.25 ml). After 5 min, acetone (500 uL) was added, and the reaction mixture was stirred for 3 h at −78° C. The resulting reaction mixture was poured into a sat'd NaH₂PO₄ and extracted with EtOAc. The organic layer was dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified through flash chromatography (4:1; Hexane:EtOAc) to give 2-((1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino)-6,6-dimethyl-7-oxa-1-thia-3-azaspiro[4.4]non-2-en-4-one as a white solid. (MS (ES⁺): 295 (M+H)⁺), and 5-((1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino)-4-thia-6-azaspiro[2.4]hept-5-en-7-one as a white solid. MS (ES⁺): 237 (M+H)⁺.

Example 157 2-(2-(Bicyclo[2.2.1]heptan-2-ylamino)-4-oxo-4,5-dihydrothiazol-5-yl)acetic acid

Method OO

A stirred mixture of (±)-exo-1-(bicyclo[2.2.1]heptan-2-yl)thiourea (1.00 g, 5.87 mmol) and maleic anhydride (576 mg, 5.87 mmol) in glacial acetic acid (20 mL) was heated to reflux. After 1 h, the solvent was evaporated in vacuo, and the residue was azeotroped from toluene (3×15 mL). The resulting solid was suspended in water, filtered, washed with water (3×15 mL) and then hexane (2×10 mL). Air drying the solid afforded the title compound (1.57 g) as a cream-colored amorphous solid.

Example 158 5-(2-(Azepan-1-yl)-2-oxoethyl)-(±)-exo-2-(bicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one

To a stirred solution of 2-(2-(bicyclo[2.2.1]heptan-2-ylamino)-4-oxo-4,5-dihydrothiazol-5-yl)acetic acid (518 mg, 1.93 mmol) in N,N-dimethylformamide (20 mL) were added N,N-diisopropylethylamine (0.404 mL, 2.32 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (807 mg, 2.12 mmol) at room temperature. After 20 min, hexamethyleneimine (0.218 mL, 1.93 mmol) was added. After an additional 3 h, the reaction was diluted with ethyl acetate (40 mL), washed with water (25 mL), and then brine (30 mL). The organic layer was then dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (SiO₂, dichloromethane/methanol, 98:2 to 97:3) to afford the title compound (472 mg) as a cream-colored amorphous solid. MS (ESI, pos. ion) m/z: 350.2 (M+H).

Example 159 2-(2-(Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)ethyl isonicotinate

Method PP

A mixture of 2-(bicyclo[2.2.1]heptan-2-ylamino)-5-(2-hydroxyethyl)-5-methylthiazol-4(5H)-one (0.080 g, 0.30 mmol), isonicotinoyl chloride hydrochloride (0.056, 0.30 mmol), and N,N-diisopropylethylamine (0.13 mL, 0.75 mmol) in CH₂Cl₂ (1.0 mL) was heated in a sealed tube in a microwave oven (SmithSynthesizer from Personal Chemistry) at 120° C. for 10 min. The reaction mixture was conc. in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was separated, washed with brine, conc. in vacuo, and purified by RP-HPLC to give the title compound as a white solid. MS m/z: 374.1 (M+H)⁺.

Example 160 2-((2S)-Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-((1-(3-(2-morpholinoethoxy)benzoyl)piperidin-4-yl)methyl)thiazol-4(5H)-one

(a) 4.0-4.7 M HCl/EtOAc, room temperature; (b) RCOOH, EDCI, HOBt or (RCO)₂O, (Et)₃N; (c) (ClCH₂CH₂)₂O, KI, K₂CO₃

5-((1-(3-(2-Aminoethoxy)benzoyl)piperidin-4-yl)methyl)-2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one

The title compound was prepared according to the procedure described in the preparation of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one by using tert-butyl 2-(3-(4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carbonyl)phenoxy)ethylcarbamate (689 mg, 1.18 mmol) as the starting material. The title compound was obtained as an off-white solid (531 mg). MS (ESI, pos. ion) m/z: 485 (M+H)

N-(2-(3-(4-((2-((2S)-Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carbonyl)phenoxy)ethyl)furan-3-carboxamide

The title compound was prepared according to the procedure described in the preparation of tert-butyl 2-(3-(4-((2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)methyl)piperidine-1-carbonyl)phenoxy)ethylcarbamate by using 5-((1-(3-(2-aminoethoxy)benzoyl)piperidin-4-yl)methyl)-2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one (93 mg, 0.19 mmol), 3-furoic acid (Aldrich, 39 mg, 0.35 mmol), EDCI (Aldrich, 74 mg, 0.38 mmol), HOBt (Aldrich, 5.2 mg, 0.038 mmol) and triethylamine (Aldrich, 39 mg, 0.38 mmol, 2.0 eq). The title compound was obtained as an off-white solid (89 mg). MS (ESI, pos. ion) m/z. 579 (M+H).

2-((2S)-Bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-((1-(3-(2-morpholinoethoxy)benzoyl)piperidin-4-yl)methyl)thiazol-4(5H)-one

A mixture of 5-((1-(3-(2-aminoethoxy)benzoyl)piperidin-4-yl)methyl)-2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methylthiazol-4(5H)-one (100 mg, 0.207 mmol), K₂CO₃ (114 mg, 0.83 mmol), KI (Aldrich, 6.9 mg, 0.041 mmol), 1-chloro-2-(2-chloroethoxy)ethane (Aldrich, 38 mg, 0.27 mmol) in CH₂Cl₂ (3 mL) was heated at reflux for 10 d. Saturated NaHCO₃ (50 mL) was added, and the crude product was extracted with CH₂Cl₂ (4×60 mL). The combined organic layers were washed with brine, dried over Na₂SO₄, filtered, and concentrated in vacuo. Flash column chromatography (silica gel, CH₂Cl₂ with 0-4% MeOH) afforded the title compound as a colorless thin film (10 mg). MS (ESI, pos. ion) m/z: 555 (M+H).

The following compounds were prepared using the methodologies outlined above.

TABLE 1 Mol Mass Methods of Structure Wt. Spec Name Prep.

280.3 281 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7-oxa-1-thia-3- azaspiro[4.4]non-2-ene-4,6- dione X

266.4 267 2-((1R,2R,4S)- bicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one Y AA

252.4 253. 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-isopropylthiazol- 4(5H)-one Y

278.4 279 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-cyclopentylthiazol- 4(5H)-one X

292.4 293 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-cyclohexylthiazol- 4(5H)-one X

292.4 293 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-cyclopentyl-5- methylthiazol-4(5H)-one AA

306.5 307 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-cyclohexyl-5- methylthiazol-4(5H)-one AA

266.4 267 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5 -tert-butylthiazol- 4(5H)-one X

266.4 267 2-(cyclohexylamino)-5- cyclopentylthiazol-4(5H)-one P X

278.3 279 5-cyclopentyl-2-(2- fluorophenylamino)thiazol- 4(5H)-one X

294.5 295 2-(cyclooctylamino)-5- cyclopentylthiazol-4(5H)-one P X

318.5 319 2-(adamantylamino)-5- cyclopentylthiazol-4(5H)-one P X

280.4 281 2-(cyclohexylmethylamino)-5- cyclopentylthiazol-4(5H)-one P X

296.3 297 5-cyclopentyl-2-(2,4- difluorophenylamino)thiazol- 4(5H)-one X

308.5 309 5-cyclohexyl-2- (cyclooctylamino)thiazol- 4(5H)-one P X

332.5 333 2-(adamantylamino)-5- cyclohexylthiazol-4(5H)-one X

280.4 281 5-cyclohexyl-2- (cyclohexylamino)thiazol- 4(5H)-one P X

292.4 293 5-cyclohexyl-2-(2- fluorophenylamino)thiazol- 4(5H)-one X

270.4 271 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-fluoro-5- isopropylthiazol-4(5H)-one Y BB

274.4 275 2-(o-toluidino)-5- cyclopentylthiazol-4(5H)-one X

296.3 297 5-cyclopentyl-5-fluoro-2-(2- fluorophenylamino)thiazol- 4(5H)-one X BB

292.4 293 2-(o-toluidino)-5-cyclopentyl-5- fluorothiazol-4(5H)-one X BB

274.4 275 2-(o-toluidino)-5- cyclopentylthiazol-4(5H)-one X

288.4 289 2-(o-toluidino)-5- cyclohexylthiazol-4(5H)-one X

268.3 269 methyl 2-(2- fluorophenylamino)-4-oxo-4,5- dihydrothiazole-5-carboxylate X

292.4 293 5-cyclopentyl-2-(2- fluorophenylamino)-5- methylthiazol-4(5H)-one AA

294.3 295 2-(2-fluorophenylamino)-5- (tetrahydro-2H-pyran-4- yl)thiazol-4(5H)-one L X

310.8 311 2-(2-chlorophenylamino)-5- (tetrahydro-2H-pyran-4- yl)thiazol-4(5H)-one L X

290.4 291 2-(o-toluidino)-5-(tetrahydro- 2H-pyran-4-yl)thiazol-4(5H)- one L X

294.8 295 2-(2-chlorophenylamino)-5- cyclopentylthiazol-4(5H)-one X

308.8 309 2-(2-chlorophenylamino)-5- cyclohexylthiazol-4(5H)-one X

296.4 297 2-(cyclohexylmethylamino)-5- (tetrahydro-2H-pyran-4- yl)thiazol-4(5H)-one P L X

308.4 309 2-(2-fluorophenylamino)-5- methyl-5-(tetrahydro-2H-pyran- 4-yl)thiazol-4(5H)-one L X AA

324.8 325 2-(2-chlorophenylamino)-5- methyl-5-(tetrahydro-2H-pyran- 4-yl)thiazol-4(5H)-one L X AA

304.4 305 2-(o-toluidino)-5-methyl-5- (tetrahydro-2H-pyran-4- yl)thiazol-4(5H)-one L X AA

280.3 281 2-(2-fluorophenylamino)-5- ((S)-tetrahydrofuran-3- yl)thiazol-4(5H)-one L X

296.8 297 2-(2-chlorophenylamino)-5- ((S)-tetrahydrofuran-3- yl)thiazol-4(5H)-one L X

294.3 295 2-(2-fluorophenylamino)-5- methyl-5-((S)-tetrahydrofuran- 3-yl)thiazol-4(5H)-one L X AA

310.8 311 2-(2-chlorophenylamino)-5- methyl-5-((S)-tetrahydrofuran- 3-yl)thiazol-4(5H)-one L X AA

280.4 281 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((S)- tetrahydrofuran-3-yl)thiazol- 4(5H)-one L X

282.4 283 2-(cyclohexylmethylamino)-5- ((S)-tetrahydrofuran-3- yl)thiazol-4(5H)-one P L X

294.4 295 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((S)- tetrahydrofuran-3-yl)thiazol- 4(5H)-one L X AA

296.4 297 2-(cyclohexylmethylamino)-5- methyl-5-((S)-tetrahydrofuran- 3-yl)thiazol-4(5H)-one P L X AA

294.4 295 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(tetrahydro-2H- pyran-4-yl)thiazol-4(5H)-one L X

308.4 309 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- (tetrahydro-2H-pyran-4- yl)thiazol-4(5H)-one L X AA

310.5 311 2-(cyclohexylmethylamino)-5- methyl-5-(tetrahydro-2H-pyran- 4-yl)thiazol-4(5H)-one P L X AA

280.3 281 2-(2-fluorophenylamino)-5- ((R)-tetrahydrofuran-3- yl)thiazol-4(5H)-one L X

296.8 297 2-(2-chlorophenylamino)-5- ((R)-tetrahydrofuran-3- yl)thiazol-4(5H)-one L X

280.4 281 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((R)- tetrahydrofuran-3-yl)thiazol- 4(5H)-one L X

282.4 283 2-(cyclohexylmethylamino)-5- ((R)-tetrahydrofuran-3- yl)thiazol-4(5H)-one P L X

294.4 295 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((R)- tetrahydrofuran-3-yl)thiazol- 4(5H)-one L X AA

296.4 297 2-(cyclohexylmethylamino)-5- methyl-5-((R)-tetrahydrofuran- 3-yl)thiazol-4(5H)-one P L X AA

310.8 311 2-(2-chlorophenylamino)-5- methyl-5-((R)-tetrahydrofuran- 3-yl)thiazol-4(5H)-one L X AA

294.3 295 2-(2-fluorophenylamino)-5- methyl-5-((R)-tetrahydrofuran- 3-yl)thiazol-4(5H)-one L X AA

393.5 338; (M-t- Bu)⁺ tert-butyl 3-(2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5-yl)pyrrolidine- 1-carboxylate L X AA

293.4 294 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- (pyrrolidin-3-yl)thiazol-4(5H)- one L X AA MM

335.5 336 5-(1-acetylpyrrolidin-3-yl)-2- ((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one L X AA MM

409.9 354; (M-t- Bu)⁺ tert-butyl 3-(2-(2- chlorophenylamino)-5-methyl- 4-oxo-4,5-dihydrothiazol-5- yl)pyrrolidine-1-carboxylate L X AA

308.4 309 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- ((tetrahydrofuran-3- yl)methyl)thiazol-4(5H)-one X AA

276.4 277 5-isopropyl-2-(2-phenylpropan- 2-ylamino)thiazol-4(5H)-one O X

290.4 291 5-isopropyl-5-methyl-2-(2- phenylpropan-2- ylamino)thiazol-4(5H)-one O X AA

282.8 283 2-(2-chlorobenzylamino)-5- isopropylthiazol-4(5H)-one O X

296.8 297 2-(2-chlorobenzylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one O X AA

310.8 311 2-(2-(2-chlorophenyl)propan-2- ylamino)-5-isopropylthiazol- 4(5H)-one R O X

324.9 325 2-(2-(2-chlorophenyl)propan-2- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one R O X AA

359.9 360 2-(2-(2-chlorophenyl)propan-2- ylamino)-5-methyl-5-(pyridin- 4-yl)thiazol-4(5H)-one R L O X

248.3 249 2-(benzylamino)-5- isopropylthiazol-4(5H)-one O X

268.8 269 2-(2-(2-chlorophenyl)propan-2- ylamino)thiazol-4(5H)-one O X

262.4 263 2-(benzylamino)-5-isopropyl-5- methylthiazol-4(5H)-one O X AA

296.8 297 2-(2-chlorophenethylamino)-5- isopropylthiazol-4(5H)-one O X

310.8 311 2-(2-chlorophenethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one O X AA

262.4 263 5-isopropyl-2-((R)-1- phenylethylamino)thiazol- 4(5H)-one O X

262.4 263 5-isopropyl-2-((S)-1- phenylethylamino)thiazol- 4(5H)-one O X

276.4 277 5-isopropyl-5-methyl-2-((R)-1- phenylethylamino)thiazol- 4(5H)-one O X AA

496.1 496 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(2- chlorophenylsulfonyl)piperidin- 4-yl)methyl)-5-methylthiazol- 4(5H)-one O X AA MM

497.6 498 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(2,6- difluorophenylsulfonyl)piperidin- 4-yl)methyl)-5-methylthiazol- 4(5H)-one O X AA MM

482.1 482 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1-(2- chlorophenylsulfonyl)piperidin- 4-yl)-5-methylthiazol-4(5H)- one O X L MM

280.4 281 2-((S)-1-(2- fluorophenyl)ethylamino)-5- isopropylthiazol-4(5H)-one Z

398.4 399 bis(trifluoromethyl)phenyl)ethyl amino)-5-isopropylthiazol- 4(5H)-one Z

330.4 331 5-isopropyl-2-((S)-1-(4- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z

330.1 331 5-isopropyl-2-((S)-1-(2- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z

412.4 413 2-((S)-1-(3,5- bis(trifluoromethyl)phenyl)ethyl amino)-5-isopropyl-5- methylthiazol-4(5H)-one Z

344.4 345 5-isopropyl-5-methyl-2-((S)-1- (4- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z

280.4 281 2-((S)-1-(4- fluorophenyl)ethylamino)-5- isopropylthiazol-4(5H)-one Z

276.4 277 (R)-5-isopropyl-5-methyl-2- ((S)-1- phenylethylamino)thiazol- 4(5H)-one Z AA

276.4 277 (S)-5-isopropyl-5-methyl-2- ((S)-1- phenylethylamino)thiazol- 4(5H)-one Z AA

252.4 253 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-isopropylthiazol- 4(5H)-one S X

330.4 331 5-isopropyl-2-((R)-1-(2- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z

280.4 281 2-((R)-1-(2- fluorophenyl)ethylamino)-5- isopropylthiazol-4(5H)-one Z

280.4 281 2-((R)-1-(4- fluorophenyl)ethylamino)-5- isopropylthiazol-4(5H)-one Z

292.3 293 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)- one S X CC

358.4 359 2-((S)-1-(2- (trifluoromethyl)phenyl)ethyl amino))-8-oxa-1-thia-3- azaspiro[4.5]non-2-ene-4-one O X EE

344.4 345 (S)-5-isopropyl-5-methyl-2- ((S)-1-(2- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z AA

344.4 345 (R)-5-isopropyl-5-methyl-2- ((S)-1-(2- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z AA

266.4 267 (S)-2-(bicyclo[2.2.1]heptan-1- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one S X AA

266.4 267 (R)-2-(bicyclo[2.2.1]heptan-1- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one S X AA

294.4 295 (S)-2-((S)-1-(2- fluorophenyl)ethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one Z AA

294.4 295 (R)-2-((S)-1-(2- fluorophenyl)ethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one Z AA

308.4 309 2-((S)-1-(2- fluorophenyl)ethylamino))-8- oxa-1-thia-3-azaspiro[4.5]non- 2-ene-4-one O X EE

252.3 253 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one O X

292.3 293 (R)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)- one O Y CC

292.3 293 (S)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)- one O Y CC

344.4 345 5-isopropyl-5-methyl-2-((R)-1- (2- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one Z AA

294.4 295 2-((R)-1-(2- fluorophenyl)ethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one Z AA

294.4 295 2-((R)-1-(4- fluorophenyl)ethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one Z AA

252.3 253 2-((S)-1-(2- fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one Z

292.4 293 2-((S)-1-(2- fluorophenyl)ethylamino))-1- thia-3-azaspiro[4.4]non-2-ene- 4-one O X

320.3 321 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5- (trifluoromethyl)thiazol-4(5H)- one O X CC

294.4 295 (S)-2-((S)-1-(4- fluorophenyl)ethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one X AA

294.4 295 (R)-2-((S)-1-(4- fluorophenyl)ethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one X AA

234.3 235 5-methyl-2-((S)-1- phenylethylamino)thiazol- 4(5H)-one O X

302.3 303 5-methyl-2-((S)-1- phenylethylamino)-5- (trifluoromethyl)thiazol-4(5H)- one O X CC

320.4 321 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5- (trifluoromethyl)thiazol-4(5H)- one O X CC

280.4 281 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-ethyl-5- isopropylthiazol-4(5H)-one O X AA

320.3 321 (R)-2-((S)-1-(2- fluorophenyl)ethylamino)-5- methyl-5- (trifluoromethyl)thiazol-4(5H)- one O Y CC

320.3 321 (S)-2-((S)-1-(2- fluorophenyl)ethylamino)-5- methyl-5- (trifluoromethyl)thiazol-4(5H)- one O Y CC

266.4 267 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylmethylamino)-5- isopropylthiazol-4(5H)-one W O X

238.3 239 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylmethylamino)-5- methylthiazol-4(5H)-one W O Y

316.3 317 5-isopropyl-2-((S)-2,2,2- trifluoro-1- phenylethylamino)thiazol- 4(5H)-one Z

278.4 279 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2- ylmethylamino)-1-thia-3- azaspiro[4.4]non-2-ene-4-one W O X

306.3 307 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylmethylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)- one W O Y CC

260.3 261 2-(5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Q O Y

328.3 329 2-(5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)- one Q O Y CC

282.4 283 ethyl 2-((1S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-4-oxo-4,5- dihydrothiazole-5-carboxylate X

298.4 299 2-((1S,4R)-Bicyclo[2.2.1]hept- 2-ylamino)-1,4-dioxo-4,5- dihydro-1H-1λ⁴-thiazole-5- carboxylic acid ethyl ester X

332.3 333 ethyl 4-oxo-2-(2- (trifluoromethyl)phenylamino)- 4,5-dihydrothiazole-5- carboxylate X

432.4 433 ethyl 5-(3-ethoxy-3-oxopropyl)- 4-oxo-2-(2- (trifluoromethyl)phenylamino)- 4,5-dihydrothiazole-5- carboxylate X DD

266.4 267 2-((1R,2R,4S)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- propylthiazol-4(5H)-one X

306.4 307 2-((1R,2R,4S)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2,2,2- trifluoroethyl)thiazol-4(5H)-one X

343.3 344 2-(2-Trifluoromethyl- phenylamino)-1-thia-3,7-diaza- spiro[4.5]dec-2-ene-4,6-dione M X

293.4 294 2-((1R,2R,4S)- Bicyclo[2.2.1]hept-2-ylamino)- 1-thia-3,7-diaza-spiro[4.5]dec- 2-ene-4,6-dione M X

388.4 389 tert-butyl 3-(4-oxo-2-(2- (trifluoromethyl)phenylamino)- 4,5-dihydrothiazol-5- yl)propanoate X DD

293.4 294 2-((1S,2S,4R)- Bicyclo[2.2.1]hept-2-ylamino)- 1-thia-3,7-diaza-spiro[4.5]dec- 2-ene-4,6-dione M X

332.3 333 3-(4-oxo-2-(2- (trifluoromethyl)phenylamino)- 4,5-dihydrothiazol-5- yl)propanoic acid X DD

240.7 241 2-(2-chlorophenylamino)-5- methylthiazol-4(5H)-one X

387.4 388 N-isobutyl-3-(4-oxo-2-(2- (trifluoromethyl)phenylamino)- 4,5-dihydrothiazol-5- yl)propanamide X DD MM

407.4 408 3-(4-oxo-2-(2- (trifluoromethyl)phenylamino)- 4,5-dihydrothiazol-5-yl)-N- phenylpropanamide X DD MM

399.4 400 5-(3-oxo-3-(piperidin-1- yl)propyl)-2-(2- (trifluoromethyl)phenylamino) thiazol-4(5H)-one X DD MM

433.4 434 5-(3-(isoindolin-2-yl)-3- oxopropyl)-2-(2- (trifluoromethyl)phenylamino) thiazol-4(5H)-one X DD MM

301.4 302 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(pyridin- 4-yl)thiazol-4(5H)-one M X

351.4 352 5-methyl-5-(pyridin-4-yl)-2-(2- (trifluoromethyl)phenylamino) thiazol-4(5H)-one M X

317.8 318 2-(2-chlorophenylamino)-5- methyl-5-(pyridin-4-yl)thiazol- 4(5H)-one M X

301.3 302 2-(2-fluorophenylamino)-5- methyl-5-(pyridin-4-yl)thiazol- 4(5H)-one M X

415.6 416 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(furan-4- carbonyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one X AA MM

506.7 507 tert-butyl 1-(4-((2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5- yl)methyl)piperidin-1-yl)-2- methyl-1-oxopropan-2- ylcarbamate X AA MM

406 407 5-((1-(2-amino-2- methylpropanoyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one X AA MM

289.4 290 2-(cyclohexylamino)-5-methyl- 5-(pyridin-4-yl)thiazol-4(5H)- one M X

341.5 342 2-(Adamantan-1-ylamino)-5- methyl-5-pyridin-4-yl-thiazol- 4-one M X

303.4 304 2-(cyclohexylmethylamino)-5- methyl-5-(pyridin-4-yl)thiazol- 4(5H)-one M X

301.4 302 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(pyridin- 3-yl)thiazol-4(5H)-one M X

317.8 318 2-(2-chlorophenylamino)-5- methyl-5-(pyridin-3-yl)thiazol- 4(5H)-one M X

317.8 318 2-(2-chlorophenylamino)-5- methyl-5-(pyridin-2-yl)thiazol- 4(5H)-one M X

301.4 302 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(pyridin- 2-yl)thiazol-4(5H)-one M X

433.6 434 5-((1-(1,2,3-thiadiazole-4- carbonyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one X AA MM

430.6 431 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-(5- methylisoxazole-3- carbonyl)piperidin-4- yl)methyl)thiazol-4(5H)-one X AA MM

444.6 445 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(3,5- dimethylisoxazole-4- carbonyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one X AA MM

416.5 417 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(isoxazole-5- carbonyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one X AA MM

429.6 430 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-(1- methyl-1H-imidazole-4- carbonyl)piperidin-4- yl)methyl)thiazol-4(5H)-one X AA MM

464.6 465 5-((1-(1H-indole-3- carbonyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one X AA MM

464.6 465 5-((1-(1H-indole-2- carbonyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one X AA MM

407.6 408 tert-butyl 4-(2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5-yl)piperidine- 1-carboxylate L X AA

307.2 308 2-((1S,2S,4R)- bicyclo [2.2.1]heptan-2- ylamino)-5-methyl-5- (piperidin-4-yl)thiazol-4(5H)- one L X AA MM(a)

349.5 350 5-(1-acetylpiperidin-4-yl)-2- ((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one L X AA MM

401.5 402 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1-(furan-4- carbonyl)piperidin-4-yl)-5- methylthiazol-4(5H)-one L X AA MM

412.6 413 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- isonicotinoylpiperidin-4-yl)-5- methylthiazol-4(5H)-one L X AA MM

412.6 413 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1- nicotinoylpiperidin-4- yl)thiazol-4(5H)-one L X AA MM

412.6 413 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1- picolinoylpiperidin-4- yl)thiazol-4(5H)-one L X AA MM

426.6 427 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(2- (pyridin-4-yl)acetyl)piperidin- 4-yl)thiazol-4(5H)-one L X AA MM

426.6 427 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(2- (pyridin-3-yl)acetyl)piperidin- 4-yl)thiazol-4(5H)-one L X AA MM

440.6 441 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(3- (pyridin-3- yl)propanoyl)piperidin-4- yl)thiazol-4(5H)-one L X AA MM

403.6 404 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- (cyclopentanecarbonyl)piperidin- 4-yl)-5-methylthiazol-4(5H)- one L X AA MM

439.6 440 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(3- phenylpropanoyl)piperidin-4- yl)thiazol-4(5H)-one L X AA MM

375.6 376 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- cyclopentylpiperidin-4-yl)-5- methylthiazol-4(5H)-one L X AA JJ

409.9 408 tert-butyl 4-(2-(2- chlorophenylamino)-4-oxo-4,5- dihydrothiazol-5-yl)piperidine- 1-carboxylate L X

357.5 358 2-(3-Hydroxy-adamantan-1- ylamino)-5-methyl-5-pyridin-4- yl-thiazol-4-one O M X

411.6 412 5-(1-benzoylpiperidin-4-yl)-2- ((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one L X AA MM

418.6 419 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1- (thiazole-4-carbonyl)piperidin- 4-yl)thiazol-4(5H)-one L X AA MM

416.5 417 2-((1S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(5- methylisoxazole-3- carbonyl)piperidin-4-yl)thiazol- 4(5H)-one L X AA MM

457.6 458 2-((1S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1-(3-(4- fluorophenyl)propanoyl)piperidin- 4-yl)-5-methylthiazol-4(5H)- one L X AA MM

468.6 469 N-(3-(4-(2-((1S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5-yl)piperidine- 1-carbonyl)phenyl)acetamide L X AA MM

317.4 318 2-((1S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(2-methoxypyridin- 4-yl)thiazol-4(5H)-one L X AA

468.6 469 N-(4-(4-(2-((1S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5-yl)piperidine- 1-carbonyl)phenyl)acetamide L X AA MM

425.6 426 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(2- phenylacetyl)piperidin-4- yl)thiazol-4(5H)-one L X AA MM

429.6 430 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1-(4- fluorobenzoyl)piperidin-4-yl)- 5-methylthiazol-4(5H)-one L X AA MM

507.6 508 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(3-(4- (trifluoromethyl)phenyl)propanoyl) piperidin-4-yl)thiazol- 4(5H)-one L X AA MM

417.6 418 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1- (thiophene-4- carbonyl)piperidin-4-yl)thiazol- 4(5H)-one L X AA MM

453.6 454 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(4- phenylbutanoyl)piperidin-4- yl)thiazol-4(5H)-one L X AA MM

517.7 518 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(3-(4- (methylsulfonyl)phenyl)propanoyl) piperidin-4-yl)thiazol- 4(5H)-one L X AA MM

437.6 438 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- cinnamoylpiperidin-4-yl)-5- methylthiazol-4(5H)-one L X AA MM

301.4 302 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-methyl-5-(pyridin- 4-yl)thiazol-4(5H)-one M X

329.4 330 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5-(pyridin-4-yl)thiazol- 4(5H)-one O M X

329.4 330 2-((S)-1-(2- fluorophenyl)ethylamino)-5- methyl-5-(pyridin-4-yl)thiazol- 4(5H)-one O M X

379.4 380 5-methyl-5-(pyridin-4-yl)-2- ((S)-1-(2- (trifluoromethyl)phenyl)ethyl amino)thiazol-4(5H)-one O M X

308.4 309 5-Ethyl-2-(3-hydroxy- adamantan-1-ylamino)-5- methyl-thiazol-4-one O X

377.6 378 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- isobutyrylpiperidin-4-yl)-5- methylthiazol-4(5H)-one L X AA MM

417.5 418 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1-(3,3,3- trifluoropropanoyl)piperidin-4- yl)thiazol-4(5H)-one L X AA MM

375.5 376 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- (cyclopropanecarbonyl)piperidin- 4-yl)-5-methylthiazol-4(5H)- one L X AA MM

389.6 390 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1- (cyclobutanecarbonyl)piperidin- 4-yl)-5-methylthiazol-4(5H)- one L X AA MM

395.5 396 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1-(2-fluoro-2- methylpropanoyl)piperidin-4- yl)-5-methylthiazol-4(5H)-one L X AA MM

363.5 364 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(1- propionylpiperidin-4-yl)thiazol- 4(5H)-one L X AA MM

399.5 400 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(1-(2,2- difluoropropanoyl)piperidin-4- yl)-5-methylthiazol-4(5H)-one L X AA MM

331.4 332 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(2-methoxypyridin- 4-yl)-5-methylthiazol-4(5H)- one L X AA

329.4 330 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5-(pyridin-2-yl)thiazol- 4(5H)-one O M X

329.4 330 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5-(pyridin-3-yl)thiazol- 4(5H)-one O M X

337.4 338 2-((1R,2S,4R)-5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(pyridin- 4-yl)thiazol-4(5H)-one Q O M X

280.4 281 2-((cyclohexylmethyl)amino)- 1-thia-3-azaspiro[4.5]dec-2-en- 4-one P X

270.1 271 2-(cyclohexylmethylamino)-5- (2-hydroxyethyl)-5- methylthiazol-4(5H)-one P X

238.4 239 2-(bicyclo[2.2.1]heptan-2- ylamino)-5,5-dimethylthiazol- 4(5H)-one X

294.4 295 5-(2-hydroxyethyl)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one P X

304.5 305 2-(tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1-thia-3- azaspiro[4.4]non-2-en-4-one P L X

266.4 267 2-((cyclohexylmethyl)amino)- 1-thia-3-azaspiro [4.4]non-2-en- 4-one P L X

254.4 255 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2- hydroxyethyl)thiazol-4(5H)-one X

268.4 279 2-(Bicyclo[2.2.1]heptan-2- ylamino)-5-(2-hydroxyethyl)-5- methylthiazol-4(5H)-one X

321.4 322 8-acetyl-2-bicyclo[2.2.1]hept-2- ylamino)-1-thia-3,8- diazaspiro[4.5]dec-2-en-4-one L X

240.4 241 2-(cycloheptylamino)-5,5- dimethylthiazol-4(5H)-one P X

256.4 257 2-(cycloheptylamino)-5-(2- hydroxyethyl)thiazol-4(5H)-one P X

270.4 271 2-(cycloheptylamino)-5-(2- hydroxyethyl)-5-methylthiazol- 4(5H)-one P X

308.4 309 5-(2-Hydroxyethyl)-5-methyl- 2-(tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one P X

290.4 291 1-methyl-5- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-4-thia-6- azaspiro[2.4]hept-5-en-7-one P L X

369.5 370 2-(1-adamantylamino)-5-(2- (phenylamino)ethyl)thiazol- 4(5H)-one P X JJ

290.4 291 6-(tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-5-thia-7- azaspiro[3.4]oct-6-en-8-one P X

252.4 253 6-(cycloheptylamino)-5-thia-7- azaspiro[3.4]oct-6-en-8-one P X

280.4 281 2-(cycloheptylamino)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P X

318.5 319 2-(tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P X

252.4 253 5-((cyclohexylmethyl)amino)- 1-methyl-4-thia-6- azaspiro[2.4]hept-5-en-7-one P L X

308.4 309 2-(cyclohexylmethylamino)-5- methyl-5-(2,2,2-trifluoroethyl)- thiazol-4(5H)-one P L X

254.4 255 2-(cyclohexylmethylamino)-5- propylthiazol-4(5H)-one P X

292.4 293 5-propyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one P X

308.4 309 2-(cycloheptylamino)-5-methyl- 5-(2,2,2-trifluoroethyl)thiazol- 4(5H)-one P L X

346.4 347 5-methyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-5-(2,2,2- trifluoroethyl)-1,3-thiazol- 4(5H)-one P L X

252.4 253 2-bicyclo[2.2.1]heptan-2- ylamino)-5-propylthiazol- 4(5H)-one X

254.4 255 2-(cycloheptylamino)-5- propylthiazol-4(5H)-one X

268.4 269 2-(cyclohexylmethylamino)- 5,5-diethylthiazol-4(5H)-one P L X

268.4 269 2-(cycloheptylamino)-5,5- diethylthiazol-4(5H)-one P L X

268.4 269 2-(cyclohexylmethylamino)-5- methyl-5-propylthiazol-4(5H)- one P L X

306.5 307 5-methyl-5-propyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one P L X

254.4 255 2-(cyclohexylamino)-5-methyl- 5-propylthiazol-4(5H)-one P L X

254.4 255 2-(cyclohexylamino)-5,5- diethylthiazol-4(5H)-one P L X

294.3 295 2-(cyclohexylamino)-5-methyl- 5-(2,2,2-trifluoroethyl)thiazol- 4(5H)-one P L X

306.5 307 5,5-diethyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one P L X

240.4 241 2-(cyclohexylamino)-5-ethyl-5- methylthiazol-4(5H)-one P L X

252.4 253 2-bicyclo[2.2.1]heptan-2- ylamino)-5-ethyl-5- methylthiazol-4(5H)-one L X

292.4 293 5-ethyl-5-methyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one P L X

254.4 255 2-(cyclohexylmethylamino)-5- ethyl-5-methylthiazol-4(5H)- one P L X

264.4 265 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 1-thia-3-azaspiro[4.4]non-2-en- 4-one L X

268.4 269 2-(cycloheptylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one P X AA

280.4 281 2-(cyclooctylamino)-1-thia-3- azaspiro[4.4]non-2-en-4-one O L X

264.4 265 2-((1R,2R,4S)- bicyclo[2.2.1]hept-2-ylamino)- 1-thia-3-azaspiro[4.4]non-2-en- 4-one L X

322.4 323 2-(cyclooctylamino)-5-methyl- 5-(2,2,2-trifluoroethyl)thiazol- 4(5H)-one O L X

278.4 279 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 1-thia-3-azaspiro[4.5]dec-2-en- 4-one X

278.4 279 2-((1R,2R,4S)- cicyclo[2.2.1]hept-2-ylamino)- 1-thia-3-azaspiro[4.5]dec-2-en- 4-one X

266.4 267 6-(cyclooctylamino)-5-thia-7- azaspiro[3.4]oct-6-en-8-one O X

335.5 336 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2- (piperidin-1-yl)ethyl)thiazol- 4(5H)-one X JJ

411.5 412 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2-(3- (trifluoromethyl)phenylamino) ethyl)thiazol-4(5H)-one X JJ

377.9 378 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(3- chlorophenylamino)ethyl)-5- methylthiazol-4(5H)-one X JJ

337.5 338 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2- morpholinoethyl)thiazol-4(5H)- one X JJ

353.5 354 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(4- fluoropiperidin-1-yl)ethyl)-5- methylthiazol-4(5H)-one X JJ

371.5 372 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(4,4- difluoropiperidin-1-yl)ethyl)-5- methylthiazol-4(5H)-one X JJ

373.5 374 2-(2-(bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5-yl)ethyl isonicotinate X

353.5 354 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(3- fluoropiperidin-1-yl)ethyl)-5- methylthiazol-4(5H)-one X JJ

306.4 307 (S)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2,2,2- trifluoroethyl)thiazol-4(5H)-one L X

306.4 307 (R)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2,2,2- trifluoroethyl)thiazol-4(5H)-one L X

266.4 267 (S)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- propylthiazol-4(5H)-one L X

266.4 267 (R)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- propylthiazol-4(5H)-one L X

371.5 372 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(3,3- difluoropiperidin-1-yl)ethyl)-5- methylthiazol-4(5H)-one X JJ

357.5 358 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2- (methyl(phenyl)amino)ethyl) thiazol-4(5H)-one X JJ

349.4 350 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-(2-(2,2,2- trifluoroethylamino)ethyl)thiazol- 4(5H)-one X JJ

282.80 283/285 2-(2-chlorophenylamino)-5- methyl-5-propylthiazol-4(5H)- one L X

276.4 277 6-(tricyclo[3.3.1.0~3,7~]non-3- ylamino)-5-thia-7- azaspiro[3.4]oct-6-en-8-one O X

290.4 291 2-(tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1-thia-3- azaspiro[4.4]non-2-en-4-one O L X

278.4 279 5-ethyl-5-methyl-2- (tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1,3-thiazol-4(5H)-one O L X

292.4 293 5-methyl-5-propyl-2- (tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1,3-thiazol-4(5H)-one O L X

292.4 293 5,5-diethyl-2- (tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1,3-thiazol-4(5H)-one O L X

436.4 436/438 2-(bicyclo[2.2.1]heptan-2- ylamino)-5-(2-((3- bromophenyl)(methyl)amino) ethyl)-5-methylthiazol- 4(5H)-one X JJ

435.5 436 (3R)-ethyl 3-(2-(2- (bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5- yl)ethylamino)-4,4,4- trifluorobutanoate X JJ

278.4 279 5-(1-methylethyl)-2- (tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1,3-thiazol-4(5H)-one O X

292.4 293 5-methyl-5-(1-methylethyl)-2- (tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1,3-thiazol-4(5H)-one O X AA

308.4 309 (7R)-2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7-(methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one L X

308.4 309 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 8-(methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one L X

282.4 283 2-((cyclohexylmethyl)amino)- 8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one P X EE

348.5 349 8-(methyloxy)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

334.5 335 8-(methyloxy)-2- (tricyclo[3.3.1.0~3,7~]non-3- ylamino)-1-thia-3- azaspiro[4.5]dec-2-en-4-one O L X

310.5 311 2-((cyclohexylmethyl)amino)- 8-(methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

296.4 297 2-(cyclohexylamino)-8- (methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

310.5 311 2-(cycloheptylamino)-8- (methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

304.4 305 7-(methyloxy)-2-((2- methylphenyl)amino)-1-thia-3- azaspiro[4.5]dec-2-en-4-one L X

296.4 297 2-(cyclohexylamino)-7- (methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

310.5 311 2-((cyclohexylmethyl)amino)- 7-(methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

310.5 311 2-(cycloheptylamino)-7- (methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one P L X

324.5 325 2-(cyclooctylamino)-7- (methyloxy)-1-thia-3- azaspiro[4.5]dec-2-en-4-one O L X

374.5 375 2-(bicyclo[2.2.1]hept-2- ylamino)-5-methyl-5-(2-((6- (methyloxy)-3- pyridinyl)amino)ethyl)-1,3- thiazol-4(5H)-one X JJ

394.5 395 2-(bicyclo[2.2.1]hept-2- ylamino)-5-(2-(4- isoquinolinylamino)ethyl)-5- methyl-1,3-thiazol-4(5H)-one X JJ

308.4 309 2-bicyclo[2.2.1]hept-2- ylamino)-7-(methyloxy)-1-thia- 3-azaspiro[4.5]dec-2-en-4-one L X

346.4 347 2′-((1S,2S,4R)- bicyclo[2.21]heptan-2-ylamino- 6-fluoro-2,3-dihydro-spiro[4H- 1-benzopyran-4,5′(4′H)- thiazo]-4′-one N X

362.9 363/365 2′-((1S,2S,4R)- bicyclo[2.21]heptan-2-ylamino- 6-chloro-2,3-dihydro-spiro[4H- 1-benzopyran-4,5′(4′H)- thiazo]-4′-one N X

288.4 289 2-(5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropylthiazol- 4(5H)-one/ 2-(6,6- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropylthiazol- 4(5H)-one X

302.4 303 2-(5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one/ 2-(6,6- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one X AA

300.4 301 2-((5,5- difluorobicyclo[2.2.1]hept-2- yl)amino)-1-thia-3- azaspiro[4.4]non-2-en-4-one/ 2-((6,6- difluorobicyclo[2.2.1]hept-2- yl)amino)-1-thia-3- azaspiro[4.4]non-2-en-4-one L X

288.4 289 2-((1R,2S,4R)-5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropylthiazol- 4(5H)-one Q X

254.4 255 2-(cycloheptylamino)-5- isopropylthiazol-4(5H)-one P X

302.4 303 (R)-2-((1R,2S,4R)-5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one Q X AA

302.4 303 (S)-2-((1R,2S,4R)-5,5- difluorobicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5- methylthiazol-4(5H)-one Q X AA

278.3 279 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5- (trifluoromethyl)thiazol-4(5H)- one X

306.4 307 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-methyl-5-(2,2,2- trifluoroethyl)thiazol-4(5H)-one S L X

292.4 293 2-(S)-2-(1-(4- fluorophenyl)ethylamino)-1- thia-3-azaspiro[4.4]non-2-en-4- one O L X

334.3 335 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5-(2,2,2- trifluoroethyl)thiazol-4(5H)-one O L X

280.4 281 5-ethyl-2-((S)-1-(4- fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one O L X

268.4 269 5-isopropyl-5-methyl-2- (thiophen-2- ylmethylamino)thiazol-4(5H)- one Z

263.4 264 5-isopropyl-5-methyl-2- (pyridin-2- ylmethylamino)thiazol-4(5H)- one Z

263.4 264 5-isopropyl-5-methyl-2- (pyridin-3- ylmethylamino)thiazol-4(5H)- one Z

263.4 264 5-isopropyl-5-methyl-2- (pyridin-4- ylmethylamino)thiazol-4(5H)- one Z

249.3 — 5-isopropyl-2-(pyridin-4- ylmethylamino)thiazol-4(5H)- one Z

249.3 250 5-isopropyl-2-(pyridin-2- ylmethylamino)thiazol-4(5H)- one Z

285.4 286 5-isopropyl-2-(isoquinolin-5- ylamino)thiazol-4(5H)-one Z

277.4 278 5-isopropyl-5-methyl-2-(1- (pyridin-2- yl)ethylamino)thiazol-4(5H)- one Z

277.4 278 5-isopropyl-5-methyl-2-(1- (pyridin-4- yl)ethylamino)thiazol-4(5H)- one Z

279.4 280 2-(1-azabicyclo[2.2.2]oct-3- ylamino)-1-thia-3- azaspiro[4.4]non-2-en-4-one O Z

294.4 295 5-isopropyl-2-((1R,2R,4R)- 1,7,7- trimethylbicyclo[2.2.1]heptan- 2-ylamino)thiazol-4(5H)-one O X

308.5 309 5-isopropyl-5-methyl-2- ((1R,2R,4R)-1,7,7- trimethylbicyclo[2.2.1]heptan- 2-ylamino)thiazol-4(5H)-one O X AA

350.5 351 5-isopropyl-5-methyl-2-(4- pentylbicyclo[2.2.2]octan-1- ylamino)thiazol-4(5H)-one O X AA

420.6 421 5-isopropyl-2-(4-(4- (methylsulfonyl)phenyl)bicyclo [2.2.2]octan-1-ylamino)thiazol- 4(5H)-one V O X

377.6 378 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1- isobutylpiperidin-4-yl)methyl)- 5-methylthiazol-4(5H)-one Y LL JJ(b) MM(a)

363.5 364 5-((1-acetylpiperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

322.5 323 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5- ((tetrahydro-2H-pyran-4- yl)methyl)thiazol-4(5H)-one Y LL

383.5 384 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(isoindolin-2-yl)- 2-oxoethyl)-5-methylthiazol- 4(5H)-one Y LL DD(b) OO(b)

417.6 418 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1- (cyclopentanecarbonyl)piperidin- 4-yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

406.6 408 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(2- (dimethylamino)acetyl)piperidin- 4-yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

414.6 415 5-((1-(1H-pyrrole-2- carbonyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

426.6 427 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1- isonicotinoylpiperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

425.6 426 5-((1-benzoylpiperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

426.6 427 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1- nicotinoylpiperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

440.6 441 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-(2- (pyridin-4-yl)acetyl)piperidin- 4-yl)methyl)thiazol-4(5H)-one Y LL MM

434.6 435 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(4- (dimethylamino)butanoyl)piperidin- 4-yl)methyl)-5- methylthiazol-4(5H)-one Y LL MM

448.6 449 N-(4-(4-((2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5- yl)methyl)piperidin-1-yl)-4- oxobutyl)acetamide Y LL MM

393.5 394 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(2- methoxyacetyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

441.6 442 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(4- hydroxybenzoyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

419.6 420 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-((R)- tetrahydrofuran-2- carbonyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

419.6 420 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-((5)- tetrahydrofuran-2- carbonyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

419.6 420 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1- (tetrahydrofuran-2- carbonyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

415.6 416 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-((1-(furan-2- carbonyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

526.7 527 N-(2-(3-(4-((2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5- yl)methyl)piperidine-1- carbonyl)phenoxy)ethyl) acetamide Y LL MM

306.5 307 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5- (cyclohexylmethyl)thiazol- 4(5H)-one Y LL

406.6 407 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5,5-bis((tetrahydro- 2H-pyran-4-yl)methyl)thiazol- 4(5H)-one Y LL

377.6 378 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1- propionylpiperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

415.6 416 5-((1-(1H-pyrazole-4- carbonyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

432.6 432 5-((1-(2-(1H-tetrazol-1- yl)acetyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

415.6 416 5-((1-(1H-imidazole-2- carbonyl)piperidin-4- yl)methyl)-2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

497.6 498 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-(2- methyl-5- (trifluoromethyl)furan-4- carbonyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

431.5 432 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-methyl-5-((1-(3,3,3- trifluoropropanoyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

224.3 225 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-methylthiazol- 4(5H)-one Y

421.6 422 tert-butyl 4-((2- (bicyclo[2.2.1]heptan-1- ylamino)-5-methyl-4-oxo-4,5- dihydrothiazol-5- yl)methyl)piperidine-1- carboxylate Y LL

321.5 322 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-methyl-5- (piperidin-4-ylmethyl)thiazol- 4(5H)-one Y LL MM(a)

415.6 416 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-((1-(furan-3- carbonyl)piperidin-4- yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

363.5 364 5-((1-acetylpiperidin-4- yl)methyl)-2- (bicyclo[2.2.1]heptan-1- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

431.5 432 2-(bicyclo[2.2.1]heptan-1- ylamino)-5-methyl-5-((1-(3,3,3- trifluoropropanoyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

414.6 415 5-((1-(1H-pyrrole-2- carbonyl)piperidin-4- yl)methyl)-2- (bicyclo[2.2.1]heptan-1- ylamino)-5-methylthiazol- 4(5H)-one Y LL MM

210.2 211 2-(2- fluorophenylamino)thiazol- 4(5H)-one Y

449.6 450 tert-butyl 4-((2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-4-oxo-4,5- dihydrothiazol-5- yl)methyl)piperidine-1- carboxylate Y LL

349.5 350 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5-(piperidin-4- ylmethyl)thiazol-4(5H)-one Y LL MM(a)

443.5 444 2-((S)-1-(4- fluorophenyl)ethylamino)-5- ((1-(furan-3-carbonyl)piperidin- 4-yl)methyl)-5-methylthiazol- 4(5H)-one Y LL MM

391.5 392 5-((1-acetylpiperidin-4- yl)methyl)-2-((S)-1-(4- fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one Y LL MM

459.5 460 2-((S)-1-(4- fluorophenyl)ethylamino)-5- methyl-5-((1-(3,3,3- trifluoropropanoyl)piperidin-4- yl)methyl)thiazol-4(5H)-one Y LL MM

442.6 443 5-((1-(1H-pyrrole-2- carbonyl)piperidin-4- yl)methyl)-2-((S)-1-(4- fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one Y LL MM

335.5 336 2-(Bicyclo[2.2.1]hept-2- ylamino)-8-isobutyl-1-thia-3,8- diaza-spiro[4.5]dec-2-en-4-one Y LL

413.6 414 8-Adamantan-2-yl-2- (bicyclo[2.2.1]hept-2-ylamino)- 1-thia-3,8-diaza-spiro[4.5]dec- 2-en-4-one Y LL

268.4 269 2-((2S)-bicyclo[2.2.1]heptan-2- ylamino)-5-(1-hydroxyethyl)-5- methylthiazol-4(5H)-one Y FF

296.4 297 2-((S)-1-(4- fluorophenyl)ethylamino)-5-(1- hydroxyethyl)-5-methylthiazol- 4(5H)-one Y FF

266.4 267 5-acetyl-2-((2S)- bicyclo[2.2.1]heptan-2- ylamino)-5-methylthiazol- 4(5H)-one Y FF JJ(a)

294.4 295 5-acetyl-2-((S)-1-(4- fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one Y FF JJ(a)

288.4 289 2-((2S)-bicyclo[2.2.1]heptan-2- ylamino)-5-(1,1-difluoroethyl)- 5-methylthiazol-4(5H)-one Y FF JJ(a) GG

316.4 317 5-(1,1-difluoroethyl)-2-((S)-1- (4-fluorophenyl)ethylamino)-5- methylthiazol-4(5H)-one Y FF JJ(a) GG

278.4 279 5,5-dimethyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one X

254.4 255 2-(cyclooctylamino)-5,5- dimethyl-1,3-thiazol-4(5H)-one X

336.5 337 ethyl 5-methyl-4-oxo-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-4,5-dihydro-1,3- thiazole-5-carboxylate X

292.4 293 5-(1-methylethyl)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one X

326.5 327 5-phenyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one X

322.5 323 5-(1-methylethyl)-5- (methyloxy)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one II

264.4 265 5-methyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one X

235.3 236 5-(1-methylethyl)-2-(3- pyridinylamino)-1,3-thiazol- 4(5H)-one X

316.5 317 2-((4-cyclohexylphenyl)amino)- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

340.5 341 5-methyl-5-phenyl-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one X

264.3 265 5-(1-methylethyl)-2-((2- (methyloxy)phenyl)amino)-1,3- thiazol-4(5H)-one X

333.5 334 5-methyl-5-(1-pyrrolidinyl)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one II

321.5 322 5-(methylamino)-5-(1- methylethyl)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one II

235.3 236 5-(1-methylethyl)-2-(2- pyridinylamino)-1,3-thiazol- 4(5H)-one X

252.3 253 2-((4-fluorophenyl)amino)-5- (1-methylethyl)-1,3-thiazol- 4(5H)-one X

235.3 236 5-(1-methylethyl)-2-(4- pyridinylamino)-1,3-thiazol- 4(5H)-one X

270.3 271 2-((2,4-difluorophenyl)amino)- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

248.4 249 5-(1-methylethyl)-2-((2- methylphenyl)amino)-1,3- thiazol-4(5H)-one X

294.4 295 5-methyl-5-(methyloxy)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one X II

302.3 303 5-(1-methylethyl)-2-((2- (trifluoromethyl)phenyl)amino)- 1,3-thiazol-4(5H)-one X

282.8 283 2-((5-chloro-2- methylphenyl)amino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

264.3 265 2-((2-fluorophenyl)amino)-1- thia-3-azaspiro[4.4]non-2-en-4- one X

274.4 275 2-(1H-indazol-5-ylamino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

273.4 274 2-(1H-indol-4-ylamino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

268.4 269 2-(((1S)-1- cyclohexylethyl)amino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

268.4 269 2-(((1R)-1- cyclohexylethyl)amino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

268.4 269 2-(cyclooctylamino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

266.3 267 2-((5-fluoro-2- methylphenyl)amino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

249.3 250 5-(1-methylethyl)-2-((3-methyl- 2-pyridinyl)amino)-1,3-thiazol- 4(5H)-one X

308.4 309 5-methyl-5- ((methyloxy)methyl)-2- (tricyclo[3.3.1.1~3,7~]dec-1- ylamino)-1,3-thiazol-4(5H)-one AA

266.3 267 2-((2-fluorophenyl)amino)-5- methyl-5-(1-methylethyl)-1,3- thiazol-4(5H)-one AA

242.4 243 5-(1-methylethyl)-2-(((1S)- 1,2,2-trimethylpropyl)amino)- 1,3-thiazol-4(5H)-one X

242.4 243 5-(1-methylethyl)-2-(((1R)- 1,2,2-trimethylpropyl)amino)- 1,3-thiazol-4(5H)-one X

262.4 263 5-methyl-5-(1-methylethyl)-2- ((2-methylphenyl)amino)-1,3- thiazol-4(5H)-one AA

252.3 253 5-ethyl-2-((2- fluorophenyl)amino)-5-methyl- 1,3-thiazol-4(5H)-one X

302.3 303 5-ethyl-5-methyl-2-((2- (trifluoromethyl)phenyl)amino)- 1,3-thiazol-4(5H)-one X

266.3 267 (5S)-2-((2- fluorophenyl)amino)-5-methyl- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one AA

266.3 267 (5R)-2-((2- fluorophenyl)amino)-5-methyl- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one AA

316.4 317 5-methyl-5-(1-methylethyl)-2- ((2- (trifluoromethyl)phenyl)amino)- 1,3-thiazol-4(5H)-one AA

300.4 301 2-((2-fluorophenyl)amino)-5- methyl-5-phenyl-1,3-thiazol- 4(5H)-one X

270.3 271 2-((2,5-difluorophenyl)amino)- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

224.3 225 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-methyl-1,3-thiazol-4(5H)-one X

300.4 301 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-methyl-5-phenyl-1,3-thiazol- 4(5H)-one X

282.8 283 2-((3-chloro-2- methylphenyl)amino)-5-(1- methylethyl)-1,3-thiazol-4(5H)- one X

268.4 269 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-methyl-5- ((methyloxy)methyl)-1,3- thiazol-4(5H)-one AA

268.3 269 2-((2-fluorophenyl)amino)-5- (2-hydroxyethyl)-5-methyl-1,3- thiazol-4(5H)-one KK

242.3 243 5-(1-methylethyl)-2-(((2R)- tetrahydro-2- furanylmethyl)amino)-1,3- thiazol-4(5H)-one X

264.4 265 5-(1-methylethyl)-2-((3- (methyloxy)phenyl)amino)-1,3- thiazol-4(5H)-one X

268.8 269 2-((2-chlorophenyl)amino)-5- (1-methylethyl)-1,3-thiazol- 4(5H)-one X

278.4 279 5-(1-methylethyl)-2-((2-methyl- 5-(methyloxy)phenyl)amino)- 1,3-thiazol-4(5H)-one X

262.4 263 2-((2,5-dimethylphenyl)amino)- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

282.8 283 2-((2-chlorophenyl)amino)-5- methyl-5-(1-methylethyl)-1,3- thiazol-4(5H)-one AA

377.5 378 5-(1-methylethyl)-2-((2-methyl- 5-((2-(4- morpholinyl)ethyl)oxy)phenyl) amino)-1,3-thiazol-4(5H)-one T Z

316.8 317 2-((2-chlorophenyl)amino)-5- methyl-5-phenyl-1,3-thiazol- 4(5H)-one X

280.8 281 2-((2-chlorophenyl)amino)-1- thia-3-azaspiro[4.4]non-2-en-4- one X

278.4 279 5-(1-methylethyl)-2-((2-methyl- 3-(methyloxy)phenyl)amino)- 1,3-thiazol-4(5H)-one X

303.2 304 2-((2,6-dichlorophenyl)amino)- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

298.8 299 2-((2-chlorophenyl)amino)-5- methyl-5-(2-(methyloxy)ethyl)- 1,3-thiazol-4(5H)-one AA

284.8 285 2-((2-chlorophenyl)amino)-5- methyl-5-((methyloxy)methyl)- 1,3-thiazol-4(5H)-one AA

296.8 297 2-((3-chloro-2- methylphenyl)amino)-5-methyl- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one AA

280.4 — 2-((4-fluoro-2- methylphenyl)amino)-5-methyl- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one AA

326.5 — 2-((1S,2S,4R)- bicyclo[2.2.1]heptan-2- ylamino)-5-(2-(2- methoxyethoxy)ethyl)-5- methylthiazol-4(5H)-one AA

316.8 317 (5S)-2-((2- chlorophenyl)amino)-5-methyl- 5-phenyl-1,3-thiazol-4(5H)-one X

316.8 317 (5R)-2-((2- chlorophenyl)amino)-5-methyl- 5-phenyl-1,3-thiazol-4(5H)-one X

282.8 283 (5R)-2-((2- chlorophenyl)amino)-5-methyl- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

282.8 283 2-((2-chlorophenyl)amino)-5- methyl-5-(1-methylethyl)-1,3- thiazol-4(5H)-one X

296.4 297 2-((2-fluorophenyl)amino)-5- (1-methylethyl)-5- ((methyloxy)methyl)-1,3- thiazol-4(5H)-one AA

303.2 304 2-((2,4-dichlorophenyl)amino)- 5-(1-methylethyl)-1,3-thiazol- 4(5H)-one X

280.4 281 2-((1R,2R,4S)- bicyclo[2.2.1]hept-2-ylamino)- 8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one EE

280.4 281 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one EE

294.4 295 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7-(methyloxy)-1-thia-3- azaspiro[4.4]non-2-en-4-one EE

310.8 311 2-((2-chlorophenyl)amino)-7- (methyloxy)-1-thia-3- azaspiro[4.4]non-2-en-4-one EE

305.4 306 2-((2-methyl-1,3-benzothiazol- 5-yl)amino)-5-(1-methylethyl)- 1,3-thiazol-4(5H)-one X

326.4 327 5-(1-methylethyl)-2-((4- (phenyloxy)phenyl)amino)-1,3- thiazol-4(5H)-one X

294.8 295 2-((2-chloro-4- methylphenyl)amino)-1-thia-3- azaspiro[4.4]non-2-en-4-one X

308.4 309 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7,7-dimethyl-8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one KK

362.3 363 2-((2-bromophenyl)amino)-5- methyl-5-(4-pyridinyl)-1,3- thiazol-4(5H)-one M X

308.4 309 (5R)-2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7,7-dimethyl-8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one KK

308.4 309 (5S)-2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7,7-dimethyl-8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one KK

352.2 353 2-((2,4-dichlorophenyl)amino)- 5-methyl-5-(4-pyridinyl)-1,3- thiazol-4(5H)-one M X

331.8 332 2-((2-chloro-4- methylphenyl)amino)-5-methyl- 5-(4-pyridinyl)-1,3-thiazol- 4(5H)-one M X

236.3 237 5-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 4-thia-6-azaspiro[2.4]hept-5-en- 7-one AA

278.4 279 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 6-methyl-1-thia-3- azaspiro[4.4]non-2-en-4-one EE

294.4 295 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 6,6-dimethyl-7-oxa-1-thia-3- azaspiro[4.4]non-2-en-4-one NN

282.5 283 2-((S)-1- cyclohexylethylamino)-5- isopropyl-5-methylthiazol- 4(5H)-one AA

294.8 295 2-(((4- chlorophenyl)methyl)amino)-1- thia-3-azaspiro[4.4]non-2-en-4- one X

274.4 275 2-(((1S)-1-phenylethyl)amino)- 1-thia-3-azaspiro[4.4]non-2-en- 4-one X

324.8 325 2-((2-chlorophenyl)amino)-7,7- dimethyl-8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one KK

308.8 309 2-((1-(2- chlorophenyl)cyclopropyl)amino)- 5-(1-methylethyl)-1,3- thiazol-4(5H)-one U O X

322.9 323 2-((1-(2- chlorophenyl)cyclopropyl)amino)- 5-methyl-5-(1-methylethyl)- 1,3-thiazol-4(5H)-one AA

284.4 285 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(1-fluoro-1-methylethyl)-5- methyl-1,3-thiazol-4(5H)-one FF GG

282.4 283 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(1-hydroxy-1-methylethyl)-5- methyl-1,3-thiazol-4(5H)-one FF

355.5 356 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 7-phenyl-1-thia-3,7- diazaspiro[4.4]non-2-ene-4,6- dione X

310.4 311 2-((3- fluorotricyclo[3.3.1.1~3,7~]dec- 1-yl)amino)-5-(1-methylethyl)- 1,3-thiazol-4(5H)-one GG

324.4 325 2-((3- fluorotricyclo[3.3.1.1~3,7~]dec- 1-yl)amino)-5-methyl-5-(1- methylethyl)-1,3-thiazol-4(5H)- one GG

308.4 309 2-(bicyclo[2.2.1]hept-1- ylamino)-7,7-dimethyl-8-oxa-1- thia-3-azaspiro[4.5]dec-2-en-4- one KK

284.4 285 (5S)-2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(1-fluoro-1-methylethyl)-5- methyl-1,3-thiazol-4(5H)-one FF GG

284.4 285 (5R)-2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(1-fluoro-1-methylethyl)-5- methyl-1,3-thiazol-4(5H)-one FF GG

324.4 325 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(4-hydroxytetrahydro-2H- pyran-4-yl)-5-methyl-1,3- thiazol-4(5H)-one FF

326.4 327 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(4-fluorotetrahydro-2H- pyran-4-yl)-5-methyl-1,3- thiazol-4(5H)-one GG

336.4 337 2-(((1S)-1-(4- fluorophenyl)ethyl)amino)-7,7- dimethyl-8-oxa-1-thia-3- azaspiro[4.5]dec-2-en-4-one KK

310.4 311 2-(((1S)-1-(2- fluorophenyl)ethyl)amino)-5- (1-hydroxy-1-methylethyl)-5- methyl-1,3-thiazol-4(5H)-one FF

306.4 307 2-((1S,2S,4R)- bicyclo[2.2.1]hept-2-ylamino)- 5-(3,6-dihydro-2H-pyran-4-yl)- 5-methyl-1,3-thiazol-4(5H)-one GG

324.5 325 (5S,7R)-2-(cyclooctylamino)- 7-(methyloxy)-1-thia-3-azaspiro [4.5]dec-2-en-4-one O L X

The following compounds are encompassed by the present invention and are prepared by one of the methodologies described herein:

TABLE 2

General Methodologies QQ-YY

Method QQ

1 eq. of 3-bromopyrrolidin-2-one (J. Med. Chem. 1987, 30, 1995-1998. H. Ikuta, H. Shirota, S. Kobayashi, Y. Yamagashi, K. Yamada, I. Yamatsu, K. Katayama) and 1.0 eq. of the appropriate thiourea were dissolved in acetone and heated to reflux for 8 h. The reaction mixture was cooled to RT, NaHCO₃ (sat. solution) was added and the aqueous phase extracted with DCM. The organic phase was separated and concentrated in vacuo to give the crude product. The obtained crude product was dissolved in pyridine and a few drops of DMF were added followed by the appropriate benzoyl chloride (3.0 eq.) and the reaction mixture was shaken at RT. 10% HCl was added and the mixture extracted with DCM. The organic phase was concentrated in vacuum. Purification was performed using preparative HPLC.

Example 161 N-{2-[2-(bicyclo[2.2.1]hept-5-en-2-ylamino)-4-oxo-4,5-dihydro-1,3-thiazol-5-yl]ethyl}-6-chloronicotinamide

5-(2-aminoethyl)-2-(bicyclo[2.2.1]hept-5-en-2-ylamino)-1,3-thiazol-4(5H)-one (0.050 g, 0.199 mmol) was suspended in MeCN (1 ml). 6-chloronicotinoyl chloride (0.140 g, 0.796 mmol) dissolved in MeCN (1 ml) was added and the reaction mixture was shaken at room temperature for 18 h. Solvents were removed in vacuo. Purification was performed using preparative HPLC (System A, 20-40% MeCN over 5 min).

¹H NMR (500 MHz, Solvent) 1.44-1.79 (m, 5 H), 2.12-2.28 (m, 1 H), 2.40-2.49 (m, 1 H), 2.84-3.02 (m, 2 H), 3.56-3.65 (m, 2 H), 3.76 (d, J=7.54 Hz, 1 H), 4.37-4.47 (m, 1 H), 6.02-6.11 (m, 1 H), 6.19-6.24 (m, 1 H), 7.52-7.56 (m, 1 H), 8.15-8.20 (m, 1 H).

HPLC-MS: 93%, R_(T)=1.74 min (System A, 10-97% MeCN over 3 min), 92%, RT=1.60 min (System B, 10-97% MeCN over 3 min)

MS (ESI+) for C₁₈H₁₉N₄O₂S m/z 391 (M+H)⁺

Method RR

1.0 eq. of the appropriate thiourea and maleic anhydride (1.0 eq.) were heated to reflux in acetone for 5 h, yielding a white emulsion. Evaporation in vacuo afforded a white solid. The product was triturated with DCM, collected on a filter and air-dried giving the carboxylic acid product as a white powder.

The carboxylic acid (1.0 eq). and 2-chloro-1-methylpyridinium iodide (1.2 eq.), or similar coupling agent, were mixed in DCM for 10 minutes before the amine (1.0 eq.) was added followed by Et₃N (1.5 eq.). The reaction mixture was stirred at RT for 16 h. The reaction mixture was poured onto a Hydromatrix column (pretreated with 1 M HCl) and the crude product was eluted with DCM. The obtained crude product was purified by reverse phase.

Example 162 2-{2-[(cyclohexylmethyl)amino]-4-oxo-4,5-dihydro-1,3-thiazol-5-yl}-N-(cyclopropylmethyl)-N-propylacetamide

Cyclohexylmethyl thiourea (0.85 g, 4.94 mmol) and maleic anhydride (4.8 g, 4.94 mmol) were refluxed over night at 110° C. in acetic acid. The reaction was concentrated and triturated with EtOAc to give the product as a pure off-white solid. MS m/z 271 (M+H)⁺

To a suspension of {2-[(cyclohexylmethyl)amino]-4-oxo-4,5-dihydro-1,3-thiazol-5-yl}acetic acid in DCM 5 ml was added thionyl chloride 1.5 eq and the reaction stirred for 30 minutes. The secondary amine (3 eq) was added and the reaction stirred overnight. Concentration and purification by reverse phase chromatography yielded the desired product.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 0.26 (m, J=3.8, 1.10 Hz, 2 H), 0.54 (m, J=8.1, 1.22 Hz, 1 H), 0.65 (m, J=7.3 Hz, 1 H), 0.93 (m, 6 H), 1.25 (m, 3 H), 1.71 (m, 8 H), 2.82 (m, J=12.2 Hz, 1 H), 3.11 (m, 1 H), 3.23 (m, J=6.5 Hz, 2 H), 3.29 (m, 2 H), 3.42 (m, 1 H), 3.54 (m, 1 H), 4.44 (m, J=10.4, 1.7 Hz, 1 H), MS m/z 366 (M+H)⁺

HPLC 100% R_(T)=3.15 min (System A. 10-97% MeCN over 3 min), 100% R_(T)=1.60 min (System B. 2-95% MeCN over 2 min).

Method SS

The synthesis of oxazolone analogues was carried out using the procedure detailed in the scheme below.

The oxazolones (F) were prepared according to the reaction scheme above from commercially available ketones (A), α-hydroxy acids (C), or α-hydroxy esters (D).

i) To a mixture of ketone (A) (1 eq) and KCN (1.1 eq) in H₂O at 0° C. was added 40% H₂SO₄ over 40 min. After stirring the reaction for an additional 1 h at ambient temperature, diethyl ether and H₂O were added. The phases were separated, and the aqueous layer was extracted with diethyl ether. The combined organic phases were washed with brine, dried over MgSO₄, and concentrated in vacuo to yield cyanohydrine (B).

ii) The cyanohydrine (B) was dissolved in concentrated HCl and the mixture was stirred under heating for 8-48 h. The solvent was evaporated, and the residue was dried in vacuo to give the crude acid (C).

iii) To a solution of the α-hydroxy acid (C) in ethanol was added acid catalyst, and the mixture was stirred under reflux for 1-3 days. The solvent was removed to give α-hydroxy ester (D).

iv) A mixture of α-hydroxy ester (D) (1 eq) and guanidine (1-3 eq) in ethanol was stirred under reflux overnight. The solvent was removed, and the residue was purified by recrystalization from water/ethyl acetate (alternatively silica gel flash chromatography) to give 2-aminooxazolone (E).

v) A mixture of 2-aminooxazolone (E) (1 eq) and amine (2.5-3 eq) in 99.5% ethanol was heated in microwave oven for 20-120 min at 160-180° C. The solvent was removed, and the residue was purified by reverse-phase preparative HPLC to give oxazolone (F).

Spiropiperidines (H) were obtained from F′ (synthesized from the corresponding ketone A) according to the scheme above.

vi) To a solution of the benzyl protected intermediate (F′) in 2-methoxyethanol was added catalytic amounts of 5% Pd/C and the mixture was exposed to H₂ (50-60 psi) for 5-24 h. Celite was added to the reaction mixture, and after filtration and removal of the solvent crude spiropiperidine G was obtained.

vii) To a solution of spiropiperidine G (1 eq) and aldehyde (1 eq) in dichloroethane was added sodium triacetoxyborohydride (1.4 eq) and the reaction mixture was stirred at 25-50° C. overnight. The material was purified by reverse-phase preparative HPLC to give the product H.

Examples 163 2-Hydroxy-2,3-dimethylbutanenitrile

To mixture of 3-methylbutan-2-one (4.71 g, 54.7 mmol) and KCN (3.92 g, 60.2 mmol) in H₂O (10 mL) was dropwise added 40% H₂SO₄ (10 mL) over 40 min. The temperature was raised to ambient, and after stirring the reaction for 1 h, diethyl ether (25 mL) and H₂O (15 mL) were added. The aqueous layer was extracted with diethyl ether (25 mL), and the combined organic phases were washed with brine (10 mL) and dried over MgSO₄. Evaporation of the solvent yielded the product as a colorless liquid.

Example 164 2-Hydroxy-2,3-dimethylbutanoic acid

A solution of 2-hydroxy-2,3-dimethylbutanenitrile (4.71 g, 54.7 mmol) in concentrated HCl was stirred at 75° C. for 5 h and then under reflux for 8 h. The solvent was removed to give the crude title compound as an off-white solid.

Example 165 Ethyl 2-hydroxy-2,3-dimethylbutanoate

To a solution of 2-hydroxy-2,3-dimethylbutanoic acid (5.53 g, 41.8 mmol) in 99.5% ethanol (200 mL) was added 2 M HCl in diethyl ether (8 mL) and the mixture was stirred under reflux for 3 days. The solvent was carefully removed to give the crude α-hydroxy ester as a pale yellow liquid.

Example 166 2-Amino-5-isopropyl-5-methyl-1,3-oxazol-4(5H)-one

A mixture of ethyl 2-hydroxy-2,3-dimethylbutanoate (2.92 g, 18.2 mmol), guanidine hydrochloride (1.74 g, 18.2 mmol), and K₂CO₃ (2.52 g, 18.2 mmol) in 99.5% ethanol (40 mL) was stirred under reflux for 20 h. The solvent was removed, and the residue was purified by silica gel flash chromatography (ethyl acetate/methanol 9:1) to give the product as a white solid.

Example 167 2-(Cyclooctylamino)-5-isopropyl-5-methyl-1,3-oxazol-4(5H)-one

A solution of 2-amino-5-isopropyl-5-methyl-1,3-oxazol-4(5H)-one (55.7 mg, 0.357 mmol) and cyclooctylamine (147 μL, 1.07 mmol) in 99.5% ethanol (1 mL) was heated in microwave oven in a sealed tube for 40 min at 180° C. The solvent was removed, and the residue was purified by preparative reverse-phase HPLC chromatography to yield the product as a white solid.

HPLC 100%, R_(T)=2.56 (System A, 10-97% MeCN over 3 min), 100%, R_(T)=1.47 min (System B, 2-95% MeCN over 2 min).

¹H NMR (400 MHz, DMSO-d₆) δ 0.77-0.79 (m, 3 H), 0.90-0.93 (m, 3 H), 1.29 (s, 2.1 H, major rotamer), 1.31 (s, 0.9 H, minor rotamer), 1.40-1.80 (m, 14 H), 1.84-1.94 (m, 1 H), 3.67-3.77 (m, 1 H), 8.67 (d, J=7.9 Hz, 0.7 H, major isomer), 8.95 (d, J=7.9 Hz, 0.3 H, minor isomer).

MS (ESI+) for C₁₅H₂₆N₂O₂ m/z 267 (M+H)⁺.

Method TT

R and R′ are bivalent alkylene and form a 3-8 membered ring with the nitrogen to which they are attached.

The thiazalones K were prepared according to the reaction scheme above from commercially available hydrazines. To a mixture of hydrazine I (1 eq) in DCM (5 mL/mmol amine) was added ethoxycarbonylisocyanate (1.1 eq) and the mixture stirred for 1 h at ambient temperature, followed by addition of 5M aq NaOH (5 mL/mmol amine) and heating for 1-2 h at 65° C. The cooled solution was extracted twice with DCM, then the combined organic layers washed consecutively with saturated aq NaHCO₃, water and brine, and finally concentrated to give the thiourea J. Thiourea J (1 eq) was reacted with the appropriate α-bromoester (1 eq) in the presence of diisopropylethylamine (1.1 eq) in EtOH (5 mL/mmol) in the microwave oven for 1-2 h 150-155° C., or by thermal heating at 95-140° C. for several days in dioxane (1 mL/mmol) in the absence of base. Concentration followed by chromatographic purification gave the thiazalone K.

Example 168 2-(Azepan-1-ylamino)-5-isopropyl-1,3-thiazol-4(5H)-one

N-(Homopiperidine)thiourea was prepared by stirring a mixture of aminopiperidine (1.0 g, 8.8 mmol) and ethoxycarbonylisocyanate (1.1 mL, 9.7 mmol) in DCM (50 mL) for 1 h, followed by addition of 5M aq NaOH (50 mL) and heatingfor 2 h at 65° C., during which time DCM evaporates. The cooled solution was extracted twice with DCM, then the combined organic layers washed consecutively with saturated aq NaHCO₃, water and brine, and finally concentrated.

This thiourea (150 mg, 0.87 mmol) was then reacted with ethyl 2-bromoisovalerate (150 μL, 0.87 mmol) in the presence of Hunigs base (diisopropylethylamine, 160 μL, 0.96 mmol) in EtOH (4 mL) in the microwave for 1 h 15 min at 150° C. Concentration followed by purification by reversed-phase HPLC, then made basic with aq NaHCO₃, gave the product as a white solid. ¹H NMR (400 MHz, DMSO-D₆) δ ppm 0.74 (d, J=6.59 Hz, 3 H), 0.91 (d, J=6.84 Hz, 3 H), 1.52 (d, J=2.20 Hz, 4 H), 1.60 (s, 4 H), 2.26 (td, J=6.53, 4.03 Hz, 1 H), 2.80-2.86 (m, 4 H), 3.95-4.00 (m, 1 H). MS (ESI) for C₁₂H₂₁N₃OS m/z 256 (M+H).

Method UU

R′2=alkyl or aryl, R=cycloalkyl, X═O or N, Y═C, O or N

The thiazalones were prepared according to the reaction scheme above from L (L was prepared according to Method A). (iii) To a solution of L (1 eq) in CCl₄ (12 mL/mmol L) was added N-bromosuccinimide (1.5 eq) and warmed to 60-70° C. for 1 h. The warm mixture was filtered and the filtrate concentrated to give the bromo intermediate M. (iv) Reaction of M with an alcohol (10-40 eq in THF or neat) at ambient temp −70° C. for 2-24 h gave, after concentration and purification, the ethers N (X═O Y═C,O). Reaction of M with a chloroalcohol (20 eq in THF) at 60° C. for 3-24 h gave, after concentration and purification, the chloroether intermediates. Amination was performed by warming a solution of the chloroether (1 eq) in THF (0.3 mL/mmol chloroether) with an amine (0.3 mL/mmol chloroether) and a crystal of NaI either thermally at 80° C. for 4-24 h or in the microwave oven 180° C. 1 h. Concentration and purification gave the aminoethers N (X═O Y═N). Reaction of M with an amine (10-40 eq in THF or neat) at ambient temp for 10-30 min gave, after concentration and purification, the amines N (X═N Y═C,N).

Example 169 2-(Bicyclo[2.2.1]hept-2-ylamino)-5-methyl-5-(3-morpholin-4-ylpropoxy)-1,3-thiazol-4(5H)-one

To a solution of the thiazolone (150 mg, 0.67 mmol) in CCl₄ (5 mL), was added N-bromosuccinimide (143 mg, 0.80 mmol) and warmed to 60° C. After 1 h, the mixture was filtered warm and concentrated to yield 244 mg of the product as a yellow solid. THF (3 mL) and 3-chloropropanol (2.2 mL, 26.8 mmol) were added and the solution warmed to 60° C. overnight. The resulting solution was concentrated and the product was purified by reversed-phase HPLC, then made basic with aq NaHCO₃, to yield the chloroether as a colourless oil.

Morpholine (3 mL) and THF (3 mL) were added and the solution was allowed to stir at 80° C. for 4 h. The resulting solution was concentrated and the product was purified by reversed-phase HPLC, then made basic with aq NaHCO₃, to yield the product as a white solid. ¹H NMR (400 MHz, DMSO-D₆) δ ppm 1.06-1.18 (m, 3 H), 1.36-1.48 (m, 4 H), 1.58-1.64 (m, 2 H), 1.66-1.71 (m, 3 H), 2.19-2.30 (m, 8 H), 3.09-3.17 (m, 2 H), 3.37-3.45 (m, 1 H), 3.48-3.57 (m, 4 H), 3.80 (m, 0.5H), 4.05 (m, 0.5H). MS (ESI) for C₁₈H₂₉N₃O₃S m/z 368 (M+H).

Example 170 2-(Bicyclo[2.2.1]hept-2-ylamino)-6-oxa-1-thia-3-azaspiro[4.4]non-2-en-4-one

To a continuously N₂-flushed solution of the thiazolone (200 mg, 0.95 mmol) in dry THF (10 mL) was added lithium diisopropylamide (1.9 mL of a 2M solution in THF/heptane/ethyl benzene, 3.8 mmol) at −78° C. The resulting brown solution was allowed to stir 1 h at this temperature after which time (3-bromopropoxy)tert-butyldimethylsilane (0.6 mL, 2.6 mmol) was added and the solution allowed to warm to 5° C. (2.5 h). The reaction was quenched with 6 mL 2/1 MeOH/HOAc followed by addition of a saturated solution of aq NaHCO₃. The silyl-protected product (50% conversion according to HPLC) was extracted with EtOAc and the resulting solution was concentrated and the product was purified by reversed-phase HPLC. During purification, the alcohol function was deprotected to give the free alcohol.

To the free alcohol (0.17 mmol) in DCM (5 mL) was added Br₂ (10 μL, 0.17 mmol) and a drop HBr (48% aqueous) and warmed to 60° C. 1 h. The resulting solution was quenched with aq NaS₂O₄ and extracted with DCM. The product was purified by reversed-phase HPLC, then made basic with aq NaHCO₃, to yield the product as a white solid.

¹H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.09-1.19 (m, 2 H), 1.21-1.30 (m, 2 H), 1.49-1.59 (m, 2 H), 1.70-1.77 (m, 1 H), 1.93 (d, J=2.93 Hz, 1 H), 1.99-2.10 (m, 1 H), 2.22-2.32 (m, 1 H), 2.36-2.48 (m, 3 H), 2.66 (dt, J=9.22, 4.55 Hz, 1 H), 3.30-3.36 (m, 1 H), 4.04-4.14 (m, 1 H), 4.15-4.23 (m, 1 H). MS (ESI) for C₁₃H₁₈N₂O₂S m/z 267 (M+H).

Method VV

The following examples serve to illustrate the preparative procedure employed for the synthesis of thiazolone analogues containing a heterocyclic side-chain at the 5-position.

Example 171 N-(2-Aminophenyl)-2-(2-anilino-4-oxo-4,5-dihydro-1,3-thiazol-5-yl)acetamide

N-(2-Aminophenyl)-2-(2-anilino-4-oxo-4,5-dihydro-1,3-thiazol-5-yl)acetic acid, prepared using method 2 above, (30 mg, 1 eq) was dissolved in a mixture of DCM/DMF (2 mL/2 mL) and O-phenylendiamine (15 mg, 1.1 eq), and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC, 30 mg, 1.3 eq) were then added sequentially. The reaction mixture was stirred 40° C. for 2 h.Separated between DCM and H₂O, the organic layer concentrated to give a crude orange brown oil used directly in the next step: HPLC 43%, R_(T)=0.93 min (System B, 2-95% MeCN over 2 min); MS [M+H]⁺ m/z=341.

Example 172 2-Anilino-5-(1H-benzimidazol-2-ylmethyl)-1,3-thiazol-4(5H)-one

N-(2-Aminophenyl)-2-(2-anilino-4-oxo-4,5-dihydro-1,3-thiazol-5-yl)acetamide (40.8 mg, 1 eq) was taken up in HOAc (2 mL), transferred to a micro-tube and run at 100° C. for 600 s. The reaction mixture was evaporated to give 42 mg, as a crude brown oil. Purified by HP-LCMS, to the pooled fractions was added NaOH (1M) to pH=14, the MeCN was evaporated and the aqueous layer extracted with DCM/H₂O (9:1), dried and evaporated to give the title compound as an off-white powder: HPLC 99%, R_(T)=2.02 min (System A, 10-97% MeCN over 3 min), 99%, R_(T)=0.96 min (System B, 2-95% MeCN over 2 min); ¹H NMR (400 MHz, METHANOL-D4) δ ppm 3.23 (m, 1 H), 3.80 (m, 1 H), 4.70 (m, 1 H), 7.02 (m, 1 H), 7.17 (m, 3 H), 7.32 (m, 2 H), 7.50 (m, 2 H), 7.62 (m, 1 H); MS [M+H]⁺ m/z=323.

Method WW

The thiourea (1.0 eq.) and the (α-bromoester/α-bromoacid (1.0 eq.) were dissolved in acetone (alternatively water, 1,4-dioxane, THF, 2-propanol or MeCN) and heated at 60-140° C. in a sealed tube or by microwave irradiation for 15-72 hours. The solvent was removed. And the product purified by crystallization from MeOH or preparative reverse-phase HPLC.

Example 173 2-(Bicyclo[2.2.1]hept-2-ylamino)-1-thia-3-azaspiro[4.4]non-2-en-4-one

A solution of N-bicyclo[2.2.1]hept-2-ylthiourea (73.9 mg, 0.434 mmol) and methyl 1-bromocyclopentanecarboxylate (89.9 mg, 0.434 mmol) in 1,4-dioxane (600 μL) was stirred at 95° C. in a sealed tube for 20 h. The solvent was removed, and the residue was purified by silica gel flash chromatography (pentane/EtOAc, 6:4). The product-containing fractions were pooled, and the solvent was removed. Subsequent purification of the residue by preparative reverse-phase HPLC yielded the product as a white solid.

HPLC 100%, R_(T)=2.98 (System A, 10-97% MeCN over 3 min), 100%, R_(T)=1.45 min (System B, 2-95% MeCN over 2 min).

¹H NMR (400 MHz, DMSO-d₆) δ 1.04-1.19 (m, 3 H), 1.34-1.51 (m, 4 H), 1.59-1.73 (m, 3 H), 1.78-1.99 (m, 4 H), 2.08-2.25 (m, 4 H), 3.18 (m, 0.3 H, minor isomer), 3.77 (m, 0.7 H, major isomer), 9.01 (d, J=6.7 Hz, 0.7 H, major isomer), 9.68 (s br, 0.3 H, minor isomer).

MS (ESI+) for C₁₄H₂₀N₂OS m/z 265 (M+H)⁺.

Method XX

According to the above synthetic scheme, X of R″X is halogen.

5-monosubstituted thiazolones may also be further alkylated at the 5-position via the liathiated anion. The following examples illustrate how this methodology can be employed to introduce more complex side-chains.

Example 174 5-(4-Bromobutyl)-2-(cycloheptylamino)-5-methyl-1,3-thiazol-4(5H)-one

To a continuous N₂-flushed solution of 2-(cycloheptylamino)-5-methyl-1,3-thiazol-4(5H)-one hydrobromide (500 mg, 2.2 mmol) in dry THF (50 mL) was added lithium diisopropylamide (4.4 mL of a 2M solution in THF/heptane/ethyl benzene, 8.8 mmol) at −78° C. The resulting brown solution was allowed to stir 1 h at this temperature after which time 1,4-dibromobutane (2.1 mL, 17.7 mmol) was added and the solution allowed to warm to −30° C. After 1 h at this temperature, the reaction was quenched with 6 mL 2/1 MeOH/HOAc and allowed to stir overnight at rt. A saturated solution of aq. NaHCO₃ was added and the product was extracted with EtOAc and then purified on SiO₂ (gradient 4/1-1/1 hex/EtOAc) to give the bromide as a white solid. Yield 227 mg. HPLC 100% R_(T)=2.34 min (System B, 10-97% MeCN over 3 min), 100% R_(T)=2.41 min (System A, 10-97% MeCN over 3 min). ¹H NMR (400 MHz, DMSO-D6) δ ppm 1.15 (td, J=7.20, 3.66 Hz, 1 H), 1.35-1.65 (m, 14 H), 1.68-1.79 (m, 4 H), 1.82-1.91 (m, 2 H), 3.49 (t, J=6.59 Hz, 2 H), 3.95 (dd, J=8.30, 3.91 Hz, 1 H), 9.10 (d, J=7.57 Hz, 1 H). MS (ESI) for C₁₅H₂₅BrN₂OS m/z 361 (M+H).

Example 175 2-(Cycloheptylamino)-5-methyl-5-(4-morpholin-4-ylbutyl)-1,3-thiazol-4(5H)-one

The bromide intermediate 5-(4-Bromobutyl)-2-(cycloheptylamino)-5-methyl-1,3-thiazol-4(5H)-one (52 mg, 0.14 mmol), described above, was dissolved in THF (3 mL), morpholine (0.84 mmol) added and warmed to 80° C. over the weekend. Purification by preparative HPLC and made basic with aq NaHCO₃, gave the product as a colourless oil. HPLC 100% R_(T)=1.45 min (System B, 10-97% MeCN over 3 min), 100% R_(T)=1.63 min (System A, 10-97% MeCN over 3 min). ¹H NMR (400 MHz, DMSO-D6) δ ppm 0.96-1.08 (m, 1 H), 1.34-1.60 (m, 18 H), 1.82-1.90 (m, 2 H), 2.18 (t, J=6.96 Hz, 2 H), 2.24-2.32 (m, 4 H), 3.52 (m, 4 H), 3.95 (s, 1 H), 9.08 (br s, 1H). MS (ESI) for C₁₉H₃₃N₃O₂S m/z 368 (M+H).

Method YY

Example 176 5-[(dimethylamino)methyl]-5-methyl-2-[(2-methylphenyl)amino]-1,3-thiazol-4(5H)-one

To a solution of {2-[(3-chloro-2-methylphenyl)amino]-4-oxo-4,5-dihydro -1,3-thiazol-5-yl}acetic acid (1 eq) in 1,4-dioxane was added N,N-dimethylmethyleneiminium chloride (2 eq) and the resulting mixture heated in a sealed tube in a microwave reactor at 150° C. for 5 minutes. The desired product was then isolated after removal of solvent in vacuo and purification by preparative HPLC.

¹H NMR (400 MHz, DMSO-D6) δ ppm 1.42 (s, 3 H), 2.12 (s, 2H), 2.23 (s, 6H), 2.57 (d, J=14.0 Hz, 1H), 2.70 (d, J=14.0 Hz, 1H), 3.30 (s, 3H), 6.83 (d, J=7.5 Hz, 1H), 7.03 (t, J=7.5 Hz, 1H), 7.15 (t, J=7.5 Hz, 1H), 7.21 (d, J=7.5 Hz, 1H); MS (ESI) for C14H19N3OS m/z 278 (M+H).

The following table of compounds were prepared using the methodologies outlined above.

TABLE 3 Calc. Method of Structure mass Exp. mass Name Prep.

— 391 N-{2-[2- (bicyclo[2.2.1]hept- 5-en-2-ylamino)-4- oxo-4,5-dihydro- 1,3-thiazol-5- yl]ethyl}-6- chloronicotinamide QQ

311.1667 311.1654 N-{2-[2- (cyclooctylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5- yl]ethyl}acetamide trifluoroacetate QQ

375.0808 375.0809 2-[2- (bicyclo[2.2.1]hept- 5-en-2-ylamino)-4- oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2- chlorophenyl)acetamide RR

366 N-(2-chlorophenyl)- 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5- yl]acetamide trifluoroacetate RR

359.1667 359.1662 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2,6- dimethylphenyl) acetamide RR

359.1667 359.1664 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2,5- dimethylphenyl) acetamide RR

359.1667 359.1664 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2,4- dimethylphenyl) acetamide RR

399.0575 399.582 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2,5- dichlorophenyl) acetamide RR

345.1511 345.1552 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2- methylphenyl) acetamide RR

365.2137 365.2141 2-{2- [(cyclohexylmethyl) amino]-4-oxo-4,5- dihydro-1,3-thiazol- 5-yl}-N- (cyclopropylmethyl)- N-propylacetamide RR

386 2- [(cyclohexylmethyl) amino]-5-[2-(3,4- dihydroquinolin- 1(2H)-yl)-2- oxoethyl]-1,3- thiazol-4(5H)-one RR

353.1773 353.1768 2- (cycloheptylamino)- 5-[2-(3- hydroxypiperidin-1- yl)-2-oxoethyl]-1,3- thiazol-4(5H)-one RR

339.1617 339.1611 2- (cycloheptylamino)- 5-(2-morpholin-4- yl-2-oxoethyl)-1,3- thiazol-4(5H)-one RR

349.1824 349.1818 5-(2-azepan-1-yl-2- oxoethyl)-2- (bicyclo[2.2.1]hept- 2-ylamino)-1,3- thiazol-4(5H)-one RR

359.0262 359.0263 N-(2,3- dichlorophenyl)-2- [4-oxo-2- (propylamino)-4,5- dihydro-1,3-thiazol- 5-yl]acetamide RR

425.1176 425.1194 N-(4-chloro-2,5- dimethoxyphenyl)- 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5- yl]acetamide RR

345.1511 345.1514 2-[2- (cyclohexylamino)- 4-oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (4- methylphenyl) acetamide RR

409.0419 409.0413 2-[2- (bicyclo[2.2.1]hept- 5-en-2-ylamino)-4- oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (4- chlorophenyl) acetamide RR

409.0419 409.0413 2-[2- (bicyclo[2.2.1]hept- 5-en-2-ylamino)-4- oxo-4,5-dihydro- 1,3-thiazol-5-yl]-N- (2,5- dichlorophenyl) acetamide RR

283.1718 283.1731 2- (cyclooctylamino)- 5-(dimethylamino)- 5-methyl-1,3- thiazol-4(5H)-one UU

309.1875 309.1877 2- (cycloheptylamino)- 5-methyl-5- piperidm-1-yl-1,3- thiazol-4(5H)-one UU

297.1875 297.1868 2- (cyclooctylamino)- 5-isopropyl-5- (methylamino)-1,3- thiazol-4(5H)-one UU

368.2246 368.2252 2- (cycloheptylamino)- 5-methyl-5-[(3- morpholin-4- ylpropyl)amino]- 1,3-thiazol-4(5H)- one UU

424.2508 424.2503 tert-butyl 4-{[2- (cycloheptylamino)- 5-methyl-4-oxo-4,5- dihydro-1,3-thiazol- 5- yl]amino}piperidine- 1-carboxylate UU

277.124882 277.126 5- [(dimethylamino) methyl]-5-methyl-2- [(2- methylphenyl)amino]- 1,3-thiazol-4(5H)- one YY

345.151097 345.15 2-anilino-5-(2- azepan-1-yl-2- oxoethyl)-5-methyl- 1,3-thiazol-4(5H)- one RR

365.119797 365.119 2-anilino-5-[2-(1,3- dihydro-2H- isoindol-2-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

379.135447 379.136 2-anilino-5-[2-(3,4- dihydroisoquinolin- 2(1H)-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

365.2129 365.213697 5-(2-azepan-1-yl-2- oxoethyl)-2- (cycloheptylamino)- 5-methyl-1,3- thiazol-4(5H)-one RR

385.1835 385.182397 2- (cycloheptylamino)- 5-[2-(1,3-dihydro- 2H-isoindol-2-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

399.1995 399.198047 2- (cycloheptylamino)- 5-[2-(3,4- dihydroisoquinolin- 2(1H)-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

379.2275 379.229347 5-(2-azepan-1-yl-2- oxoethyl)-2- (cyclooctylamino)- 5-methyl-1,3- thiazol-4(5H)-one RR

336.1049 336.10445 2- (cyclooctylamino)- 5-[2-(1,3-dihydro- 2H-isoindol-2-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

413.2138 413.213697 2- (cyclooctylamino)- 5-[2-(3,4- dihydroquinolin- 1(2H)-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

379.1352 379.135447 2-anilino-5-[2-(3,4- dihydroquinolin- 1(2H)-yl)-2- oxoethyl]-5-methyl- 1,3-thiazol-4(5H)- one RR

264.1296 264.1307 2- (bicyclo[2.2.1]hept- 2-ylamino)-1-thia-3- azaspiro[4.4]non-2- en-4-one WW

266.1453 266.1442 2- (cycloheptylamino)- 1-thia-3- azaspiro[4.4]non-2- en-4-one WW

280.1609 280.1611 2- (cyclooctylamino)- 1-thia-3- azaspiro[4.4]non-2- en-4-one WW

266.1453 266.1445 2-[(2,2,3,3- tetramethylcyclopropyl) amino]-1-thia-3- azaspiro[4.4]non-2- en-4-one WW

266.1453 266.146 2- (bicyclo[2.2.1]hept- 2-ylamino)-5- methyl-5-propyl- 1,3-thiazol-4(5H)- one WW

268.1609 268.1618 2- (cycloheptylamino)- 5-methyl-5-propyl- 1,3-thiazol-4(5H)- one WW

282.1766 282.1774 2- (cyclooctylamino)- 5-methyl-5-propyl- 1,3-thiazol-4(5H)- one WW

268.1609 268.1609 5-methyl-5-propyl- 2-[(2,2,3,3- tetramethylcyclopropyl) amino]-1,3- thiazol-4(5H)-one WW

252.1296 252.1288 2- (bicyclo[2.2.1]hept- 2-ylamino)-5-ethyl- 5-methyl-1,3- thiazol-4(5H)-one WW

254.1453 254.1448 2- (cycloheptylamino)- 5-ethyl-S-methyl- 1,3-thiazol-4(5H)- one WW

254.1453 254.1443 5-ethyl-5-methyl-2- [(2,2,3,3- tetramethylcyclopropyl) amino]-1,3- thiazol-4(5H)-one WW

278.1453 278.1459 5-ethyl-5-methyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-thiazol-4(5H)- one WW

280.1245 278.0941 2-[(1S,2S,4R)- bicyclo[2.2.1]hept- 2-ylamino]-8-oxa-1- thia-3- azaspiro[4.5]dec-2- en-4-one WW

252.1296 252.1296 2- (bicyclo[2.2.1]hept- 1-ylamino)-5-ethyl- 5-methyl-1,3- thiazol-4(5H)-one WW

268.1609 268.1601 2- (cyclooctylamino)- 5-ethyl-5-methyl- 1,3-thiazol-4(5H)- one WW

292.1609 292.1614 5-methyl-5-propyl- 2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-thiazol-4(5H)- one WW

266.1453 266.1443 2- (bicyclo[2.2.1]hept- 2-ylamino)-5,5- diethyl-1,3-thiazol- 4(5H)-one WW

282.1766 282.1758 2- (cyclooctylamino)- 5,5-diethyl-1,3- thiazol-4(5H)-one WW

292.1609 292.1622 5,5-diethyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-thiazol-4(5H)- one WW

254.1453 254.1454 5-ethyl-5-methyl-2- [(1- methylcyclohexyl) amino]-1,3-thiazol- 4(5H)-one trifluoroacetate WW

268.1609 268.1609 5-methyl-2-[(1- methylcyclohexyl) amino]-5-propyl-1,3- thiazol-4(5H)-one trifluoroacetate WW

254.1453 254.1442 5-ethyl-5-methyl-2- [(4- methylcyclohexyl) amino]-1,3-thiazol- 4(5H)-one WW

282.1766 282.1766 5-ethyl-5-methyl-2- [(3,3,5- trimethylcyclohexyl) amino]-1,3-thiazol- 4(5H)-one WW

264.1296 264.1291 5,5-dimethyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-thiazol-4(5H)- one WW

252.1296 252.1289 2- (bicyclo[2.2.1]hept- 7-ylamino)-5-ethyl- 5-methyl-1,3- thiazol-4(5H)-one WW

266.1453 266.1459 2- (bicyclo[2.2.1]hept- 7-ylamino)-5- methyl-5-propyl- 1,3-thiazol-4(5H)- one WW

254.1453 254.1444 (5S)-2- (cycloheptylamino)- 5-ethyl-5-methyl- 1,3-thiazol-4(5H)- one WW

254.1453 254.1445 (5R)-2- (cycloheptylamino)- 5-ethyl-5-methyl- 1,3-thiazol-4(5H)- one WW

266.1453 266.144 2- (bicyclo[2.2.1]hept- 7-ylamino)-5,5- diethyl-1,3-thiazol- 4(5H)-one WW

266.1453 266.1445 2- (bicyclo[2.2.1]hept- 1-ylamino)-5,5- diethyl-1,3-thiazol- 4(5H)-one WW

266.1453 266.1445 2- (bicyclo[2.2.1]hept- 1-ylamino)-5- methyl-5-propyl- 1,3-thiazol-4(5H)- one WW

360.0871 360.0867 5-(4-bromobutyl)-2- (cycloheptylamino)- 5-methyl-1,3- thiazol-4(5H)-one XX

381.2814 381.281 2- (cycloheptylamino)- 5-[4- (diethylamino)butyl]- 5-propyl-1,3- thiazol-4(5H)-one XX

367.2293 367.2294 2- (cycloheptylamino)- 5-methyl-5-(4- morpholin-4- ylbutyl)-1,3-thiazol- 4(5H)-one XX

380.261 380.2612 2- (cycloheptylamino)- 5-methyl-5-[4-(4- methylpiperazin-1- yl)butyl]-1,3- thiazol-4(5H)-one XX

466.2978 466.2992 tert-butyl 4-{4-[2- (cycloheptylamino)- 5-methyl-4-oxo-4,5- dihydro-1,3-thiazol- 5- yl]butyl}piperazine- 1-carboxylate XX

351.198 351.1977 2- (bicyclo[2.2.1]hept- 2-ylamino)-5- methyl-5-(3- morpholin-4- ylpropyl)-1,3- thiazol-4(5H)-one XX

266.1453 266.1458 2-[(1S,2S,4R)- bicyclo[2.2.1]hept- 2-ylamino]-5,5- diethyl-1,3-thiazol- 4(5H)-one WW

270.1402 270.1401 2- (cyclooctylamino)- 5-methoxy-5- methyl-1,3-thiazol- 4(5H)-one UU

270.1402 270.139 2- (cycloheptylamino)- 5-ethoxy-5-methyl- 1,3-thiazol-4(5H)- one UU

284.1558 284.156 2- (cycloheptylamino)- 5-isopropoxy-5- methyl-1,3-thiazol- 4(5H)-one UU

298.1715 298.172 5-butoxy-2- (cycloheptylamino)- 5-methyl-1,3- thiazol-4(5H)-one UU

298.1715 298.1712 2- (cyclooctylamino)- 5-isopropyl-5- methoxy-1,3- thiazol-4(5H)-one UU

374.2028 374.2034 5-butoxy-2- (cyclooctylamino)- 5-phenyl-1,3- thiazol-4(5H)-one UU

300.1508 300.1517 2- (cycloheptylamino)- 5-(3- hydroxypropoxy)-5- methyl-1,3-thiazol- 4(5H)-one UU

296.1558 296.1558 2- (bicyclo[2.2.1]hept- 2-ylamino)-5- butoxy-5-methyl- 1,3-thiazol-4(5H)- one UU

326.2028 326.2036 5-butoxy-2- (cycloheptylamino)- 5-propyl-1,3- thiazol-4(5H)-one UU

284.1558 284.1547 2- (cycloheptylamino)- 5-methoxy-5- propyl-1,3-thiazol- 4(5H)-one UU

367.193 367.1934 2- (bicyclo[2.2.1]hept- 2-ylamino)-5- methyl-5-(3- morpholin-4- ylpropoxy)-1,3- thiazol-4(5H)-one UU

365.2137 365.2134 2- (bicyclol[2.2.1]hept- 2-ylamino)-5- methyl-5-(3- piperidin-1- ylpropoxy)-1,3- thiazol-4(5H)-one UU

466.2614 466.2619 tert-butyl 4-(3-{[2- (bicyclo[2.2.1]hept- 2-ylamino)-5- methyl-4-oxo-4,5- dihydro-1,3-thiazol- 5- yl]oxy}propyl)piperazine- 1-carboxylate UU

326.1664 326.1666 2- (cycloheptylamino)- 5-methyl-5- (tetrahydrofuran-2- ylmethoxy)-1,3- thiazol-4(5H)-one UU

358.1926 358.1917 2- (cycloheptylamino)- 5-[2-(2- ethoxyethoxy)ethoxy]- 5-methyl-1,3- thiazol-4(5H)-one UU

312.1508 312.1503 2- (cycloheptylamino)- 5-methyl-5- (tetrahydrofuran-3- yloxy)-1,3-thiazol- 4(5H)-one UU

362.1664 362.1675 2- (cycloheptylamino)- 5-methyl-5-(2- phenoxyethoxy)- 1,3-thiazol-4(5H)- one UU

324.1871 324.1869 2- (cycloheptylamino)- 5-(cyclohexyloxy)- 5-methyl-1,3- thiazol-4(5H)-one UU

266.1089 266.1076 2- (bicyclo[2.2.1]hept- 2-ylamino)-6-oxa-1- thia-3- azaspiro[4.4]non-2- en-4-one UU

323 2-anilino-5-(1H- benzimidazol-2- ylmethyl)-1,3- thiazol-4(5H)-one VV

343. 5-(1H- benzimidazol-2- ylmethyl)-2- [(cyclohexylmethyl) amino]-1,3-thiazol- 4(5H)-one VV

336.1049 336.1045 2-anilino-5-[(1- methyl-1H- benzimidazol-2- yl)methyl]-1,3- thiazol-4(5H)-one VV

255.1405 255.1397 2-(azepan-1- ylamino)-5- isopropyl-1,3- thiazol-4(5H)-one TT

255.1405 255.1401 2-(azepan-1- ylamino)-5-ethyl-5- methyl-1,3-thiazol- 4(5H)-one TT

267.1405 267.1399 5-ethyl-2- (hexahydrocyclopenta [c]pyrrol-2(1H)- ylamino)-5-methyl- 1,3-thiazol-4(5H)- one TT

269.1562 269.157 2-(azepan-1- ylamino)-5,5- diethyl-1,3-thiazol- 4(5H)-one TT

281.1562 281.1569 5,5-diethyl-2- (hexahydrocyclopenta [c]pyrrol-2(1H)- ylamino)-1,3- thiazol-4(5H)-one TT

271.1354 271.1344 5-isopropyl-2- {[(2R)-2- (methoxymethyl) pyrrolidin-1-yl]amino}- 1,3-thiazol-4(5H)- one TT

271.1354 271.1342 5-isopropyl-2-{[2- (methoxymethyl) pyrrolidin-1-yl]amino}- 1,3-thiazol-4(5H)- one TT

243.1041 243.1049 5-isopropyl-2- (morpholin-4- ylamino)-1,3- thiazol-4(5H)-one TT

269.1562 269.1553 2-[(2,6- dimethylpiperidin-1- yl)amino]-5- isopropyl-1,3- thiazol-4(5H)-one TT

253.1249 253.1249 5-ethyl-2- (hexahydrocyclopenta [c]pyrrol-2(1H)- ylamino)-1,3- thiazol-4(5H)-one TT

258.1368 258.136 2-(2,2- dimethylpyrrolidin- 1-yl)-5-phenyl-1,3- oxazol-4(5H)-one SS

222.1368 222.1373 2- (bicyclo[2.2.1]hept- 2-ylamino)-5,5- dimethyl-1,3- oxazol-4(5H)-one SS

270.1368 270.1356 2- (bicyclo[2.2.1]hept- 2-ylamino)-5- phenyl-1,3-oxazol- 4(5H)-one SS

281.1164 281.1163 5-phenyl-2-[(2- pyridin-2- ylethyl)amino]-1,3- oxazol-4(5H)-one SS

284.1525 284.1513 5-benzyl-2- (bicyclo[2.2.1]hept- 2-ylamino)-1,3- oxazol-4(5H)-one SS

300.1838 300.1843 5-benzyl-2- (cyclooctylamino)- 1,3-oxazol-4(5H)- one SS

252.1838 252.183 2- (cyclooctylamino)- 5-isopropyl-1,3- oxazol-4(5H)-one SS

290.1994 290.1986 2-(1- adamantylamino)-5- isobutyl-1,3-oxazol- 4(5H)-one SS

266.1994 266 2- (cyclooctylamino)- 5-isobutyl-1,3- oxazol-4(5H)-one SS

286.1681 286.1672 2- (cyclooctylamino)- 5-phenyl-1,3- oxazol-4(5H)-one SS

310.1681 310.169 2-(1- adamantylamino)-5- phenyl-1,3-oxazol- 4(5H)-one SS

324.1838 324.1827 2-(1- adamantylamino)-5- benzyl-1,3-oxazol- 4(5H)-one SS

276.1838 276.1844 5-isobutyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-oxazol-4(5H)- one SS

252.1838 252.1828 2- (cycloheptylamino)- 5,5-diethyl-1,3- oxazol-4(5H)-one SS

266.1994 266.1991 2- (cyclooctylamino)- 5,5-diethyl-1,3- oxazol-4(5H)-one SS

250.1681 250.1677 2- (bicyclo[2.2.1]hept- 2-ylamino)-5,5- diethyl-1,3-oxazol- 4(5H)-one SS

276.1838 276.183 5,5-diethyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-oxazol-4(5H)- one SS

290.1994 290.1987 2-(1- adamantylamino)- 5,5-diethyl-1,3- oxazol-4(5H)-one SS

262.1681 262.1675 5-isopropyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)- 1,3-oxazol-4(5H)- one SS

278.1994 278.1984 2- (cyclooctylamino)- 1-oxa-3- azaspiro[4.5]dec-2- en-4-one trifluoroacetate SS

276.1838 276.1839 2-(1- adamantylamino)-5- isopropyl-1,3- oxazol-4(5H)-one SS

276.1838 276.1832 2-(2- adamantylamino)-5- isopropyl-1,3- oxazol-4(5H)-one SS

292.1787 292.1774 2-[(3-hydroxy-1- adamantyl)amino]- 5-isopropyl-1,3- oxazol-4(5H)-one SS

290.1994 290.1995 2-(2- adamantylamino)- 5,5-diethyl-1,3- oxazol-4(5H)-one SS

306.1943 306.1953 5,5-diethyl-2-[(3- hydroxy-1- adamantyl)amino]- 1,3-oxazol-4(5H)- one SS

302.1994 302.1994 2-(2- adamantylamino)-1- oxa-3- azaspiro[4.5]dec-2- en-4-one SS

288.1838 288.1833 2-(2- adamantylamino)-1- oxa-3- azaspiro[4.4]non-2- en-4-one SS

341.2103 341.2113 8-benzyl-2- (cyclohexylamino)- 1-oxa-3,8- diazaspiro[4.5]dec- 2-en-4-one SS

248.1525 248.1519 2- (bicyclo[2.2.1lhept- 2-ylamino)-1-oxa-3- azaspiro[4.4]non-2- en-4-one SS

264.1838 264.1826 2- (cyclooctylamino)- 1-oxa-3- azaspirol[4.4]non-2- en-4-one SS

274.1681 274.1679 2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)-1- oxa-3- azaspiro[4.4]non-2- en-4-one SS

288.1838 288.1825 2-(1- adamantylamino)-1- oxa-3- azaspiro[4.4]non-2- en-4-one SS

304.1787 304.1778 2-[(3-hydroxy-1- adamantyl)amino]- 1-oxa-3- azaspiro[4.4]non-2- en-4-one SS

393.2416 393.2406 2-(2- adamantylamino)-8- benzyl-1-oxa-3,8- diazaspiro[4.5]dec- 2-en-4-one SS

316.1399 316.139 2-(2- adamantylamino)-5- methyl-5- (trifluoromethyl)- 1,3-oxazol-4(5H)- one SS

327.1947 327.1941 8-benzyl-2- (cyclopentylamino)- 1-oxa-3,8- diazaspiro[4.5]dec- 2-en-4-one SS

315.1947 315.1945 8-benzyl-2-(tert- butylamino)-1-oxa- 3,8- diazaspiro[4.5]dec- 2-en-4-one SS

292.1399 292.1397 2- (cyclooctylamino)- 5-methyl-5- (trifluoromethyl)- 1,3-oxazol-4(5H)- one SS

302.1242 302.1246 5-methyl-2- (tricyclo[3.3.1.0~3,7~] non-3-ylamino)-5- (trifluoromethyl)- 1,3-oxazol-4(5H)- one SS

335.1634 335.1628 2-anilino-8-benzyl- 1-oxa-3,8- diazaspiro[4.5]dec- 2-en-4-one SS

399.2134 399.2144 2-(2- adamantylamino)-8- (3,3,3- trifluoropropyl)-1- oxa-3,8- diazaspiro[4.5]dec- 2-en-4-one SS

General Methodologies YY-MMM

Method YY

Reference: H. Mahmud et al. Tetrahedron 57 (2001), 4905-4105.

Example 177 Methyl 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoate

A mixture of 5-(4-bromophenyl)-2-((S)-1-(4fluorophenyl)ethylamino)-5-methylthiazol-4(5H)-one (0.79 g, 1.9 mmol), triphenylphosphine (Aldrich, 0.15 g, 0.58 mmol), palladium acetate (Aldrich, 0.11 g, 0.48 mmol), potassium acetate (Aldrich, 0.24 g, 2.4 mmol), in MeOH (3 mL) and DMF (3 mL) was pressurized with carbon monoxide, purged twice with CO and then heated to 100° C. overnight at 40-50 psi of CO. After the reaction mixture was cooled to ambient temp., then contents were filtered through Celite. The Celite pad was washed with CH₂Cl₂, and the organic phase was dried over Na₂SO₄, concentrated in vacuo. The crude material was purified using silica gel chromatography. MS: 387 (M+1).

Example 178 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoic acid

To a solution of methyl 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoate (0.64 g, 1.7 mmol) in THF (3 mL), MeOH (1 mL), and H₂O (1 mL) was added lithium hydroxide monohydrate (0.10 g, 2.5 mmol), and the mixture was stirred at ambient temp. overnight. The mixture was then heated to reflux for 5 h. The mixture was neutralized with 1N HCl, and then extracted with CH₂Cl₂ five times. The organic extracts were dried over Na₂SO₄, concentrated in vacuo, and the product was dried on vacuum. MS: 373 (M+1).

Example 179 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoyl chloride

To a solution of 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoic acid (0.48 g, 1.29 mmol) in CH₂Cl₂ (6 mL) was added thionyl chloride (Aldrich, 0.19 ml, 2.58 mmol), and 2 drops of DMF. After stirring the mixture overnight at ambient temp., the crude product was concentrated in vacuo and dried on high vacuum. The product was used in next step without purification.

Example 180 2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-5-(4-(pyrrolidine-1-carbonyl)phenyl)thiazol-4(5H)-one

To a solution of 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoyl chloride (0.100 g, 0.26 mmol) in CH₂Cl₂ (1 mL) in a 0° C. bath was added pyrrolidine (Aldrich, 0.063 ml, 0.77 mmol). The mixture was gradually warmed to ambient temp. and stirred for 40 min. The reaction mixture was then added to water (5 mL), and the aqueous layer was extracted with CH₂Cl₂ three times. The combined organic phases were dried over Na₂SO₄, and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 426 (M+1).

Method ZZ

Example 181 4-(2-((S)-1-(2-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzonitrile

To a mixture of 2-((S)-1-(2-fluorophenyl)ethylamino)-5-methylthiazol-4(5H)-one (0.0500 g, 0.198 mmol), 4-bromobenzonitrile (Aldrich, 0.0721 g, 0.396 mmol), Pd₂(dba)₃ (Aldrich, 0.0127 g, 0.0139 mmol), 2-(diphenylphosphino)-1-(2-(diphenylphosphino)naphthalen-1-yl)naphthalene (Strem, 0.0123 g, 0.0198 mmol), and NaN(TMS)₂ (Aldrich, 0.0727 g, 0.396 mmol) was added toluene (2 mL) in a dry box. The mixture was gradually heated to 95° C. and stirred overnight. The reaction was cooled to ambient temp. and quenched with NH₄Cl (5 mL). The reaction mixture was extract with EtOAc. The organic phase was dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography. MS: 354 (M+1)

Method AAA

Example 182 Methyl 2-(2-methoxypyridin-4-yl)acetate

To the solution of lithium diisopropylamide (Aldrich, 2.0M, 122 mL, 244 mmol), THF (90 mL) and hexamethylphosphoric triamide (Aldrich, 16 mL, 89 mmol) at −78° C. under nitrogen was added, in 10 min, a solution of 2-methoxy-4-methylpyridine (10.0 g, 81 mmol) in THF (30 mL). After 30 min, a solution of dimethyl carbonate (Aldrich, 7.5 mL, 90 mmol) in THF (30 mL) was added over 15 min. The stirring was continued for 2 h at −78° C. before the reaction was quenched with MeOH (30 mL). The mixture was filtered through Celite and the cake was washed with EtOAc. The filtrate was concentrated in vacuo, and the crude product was purified by silica gel chromatography. MS: 182 (M+1).

Method BBB

In a 10 mL RB flask was added 5-methyl-2-(1-(thiophen-2-yl)ethylamino)-5-(trifluoromethyl)thiazol-4(5H)-one (0.200 g, 0.649 mmol) NBS (0.133 g, 0.746 mmol) and 2 mL of DMF. This mixture was stirred overnight at ambient temp. Water (10 mL) was added and the resulting precipitate, which was collected by filtration to give 2-(1-(5-bromothiophen-2-yl)ethylamino)-5-methyl-5-(trifluoromethyl)thiazol-4(5H)-one as a light yellow solid.

Method CCC

CuCN (140 mg, 1.6 mmol) and 2-((S)-1-(4-bromophenyl)ethylamino)-5-methyl-5-(trifluoromethyl)thiazol-4(5H)-one (150 mg, 0.39 mmol) and 2 mL of DMF were combined in a sealed tube and heated to 150° C. for 12 h. The residue was purified by column chromatography (10 to 60% EA/Hex, 40 g) to give 4-((S)-1-(5-methyl-4-oxo-5-(trifluoromethyl)-4,5-dihydrothiazol-2-ylamino)ethyl)benzonitrile as a slightly yellow solid.

Method DDD

A 100 mL RB was charged with 2-((1R,4R)-4-hydroxycyclohexylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (0.050 g, 0.18 mmol) and 5 mL THF. Triphenyl phosphine (0.073 g, 0.28 mmol) was added along with benzoic acid (0.034 g, 0.28 mmol), then DEAD (0.044 ml, 0.28 mmol) (at 0° C.). This solution was allowed to stir at ambient temp. for 18 h, then 3 mL of 1M NaOMe in MeOH was added, and this mixture was stirred for an additional 2 days. After that time, the solvents were removed in vacuo and the residue was dissolved in water and EtOAc. The organic layer was separated, dried and concentrated to give an oil, which was purified by column chromatography (5-10% MeOH/DCM) to give 2-((1S,4S)-4-hydroxycyclohexylamino)-5-isopropyl-5-methylthiazol-4(5H)-one as an off-white solid.

Method EEE

A 5 mL vial was charged with 2-((1S,2S)-2-(benzyloxy)cyclohexylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (0.100 g, 0.28 mmol) and 1 mL of DCM. To this was added iodotrimethylsilane (0.22 g, 1.1 mmol). The vial was sealed and heated at 65° C. for 36 h. The reaction was concentrated and purified by column chromatography (2% to 7% MeOH/DCM) to give 2-((1S,2S)-2-hydroxycyclohexylamino)-5-isopropyl-5-methylthiazol-4(5H)-one as a yellow solid

Method FFF

A 5 mL flask was charged flask with 2-((1S,3S)-3-(tert-butyldimethylsilyloxy)cyclopentylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (0.470 g, 1.3 mmol) and tetrabutylammonium fluoride, (1.0M in THF (5.1 ml, 5.1 mmol) and allowed to stir at ambient temp. overnight. The crude reaction mixture was concentrated onto silica gel and the mixture was purified by column chromatography (2-6% MeOH/DCM) to give 2-((1S,3S)-3-hydroxycyclopentylamino)-5-isopropyl-5-methylthiazol-4(5H)-one as a white solid.

Method GGG

Example 183 4-(2-((S)-1-(2-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzamide

The mixture of 4-(2-((S)-1-(2-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzonitrile (0.080 g, 0.23 mmol) and potassium hydroxide (VWR, 0.17 g, 2.9 mmol) and t-BuOH (2 mL) was gradually heated to 85° C. The solid gradually dissolved and the mixture became a solution. After 1 h, the reaction was added to 2N HCl until the pH was ca. 7-8. The mixture was extracted three times with CH₂Cl₂, and the combined organic layers was dried over Na₂SO₄, filtered, and concentrated in vacuo. The crude was purified by silica gel chromatography. MS: 372 (M+1), 370 (M−1).

Method HHH

Example 184 ((1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-yloxy)(tert-butyl)diphenylsilane

To a solution of (1R,2S,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-ol (4.20 g, 19.2 mmol) in DMF (10 mL) was added tert-butylchlorodiphenylsilane (6.00 mL, 23.1 mmol) and imidazole (3.27 g, 48.1 mmol). The resulting mixture was stirred at ambient temp. overnight. The mixture was partitioned between diethyl ether and water. The organic portion was separated, washed with brine, and concentrated in vacuo. The residue was purified by flash column chromatography (0 to 5% of EtOAc in hexanes) to give the title compound as a colorless oil.

Example 185 (1R,2S,4R,5S)-5-(tert-Butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ol

Palladium (10 wt. % on activated carbon, 1.50 g) was added to a solution of ((1R,2S,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-yloxy)(tert-butyl)diphenylsilane (8.47 g, 18.5 mmol) in methanol (50 mL). The mixture was placed under a balloon of hydrogen. After stirring at ambient temperature for 24 h, the mixture was filtered through a pad of Celite. Solvents were removed in vacuo to give the title compound as a colorless viscous oil.

Example 186 (1R,4R,5S)-5-(tert-Butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-one

Silica gel 60 (particle size, 0.040-0.063 mm, CAS # 63231-67-4, from EMD Chemical Inc., 21 g) was added to a solution of (1R,2S,4R,5S)-5-(tert butyldiphenylsilyloxy)-bicyclo[2.2.1]heptan-2-ol (6.75 g, 18.4 mmol) in anhydrous dichloromethane (100 mL). The mixture was cooled to 0° C. Pyridinium chlorochromate (6.35 g, 29.5 mmol) was added to the mixture. The reaction mixture was gradually warmed to ambient temperature and stirred at this temperature for 16 h. The mixture was diluted with dichloromethane, and filtered through a pad of silica gel. Removal of the solvents gave the title compound as a colorless viscous oil.

Example 187 (1R,2R,4R,5S)-5-(tert-Butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ol

To a solution of (1R,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-one (5.75 g, 15.8 mmol) in THF (15.0 mL) was added dropwise to L-Selectride (1.0 M solution in THF, 31.5 ml, 31.5 mmol) at −78° C. under nitrogen. The resulting mixture was stirred at −78° C. for 3 h, then quenched with tris-HCl (1M, PH 7.0 at 25° C.). The mixture was warmed to ambient temp. and partitioned between EtOAc and Tris-HCl. The combined organic portions were washed with brine, and conc. in vacuo. The residue was dissolved in MeOH (60 mL), stirred with NaOH (pellets, 3.2 g) at 60° C. overnight. After cooling to ambient temp., the solvent was removed in vacuo. The residue was partitioned between diethyl ether and water. The combined organic portions were washed with brine, dried with Na₂SO₄, filtered, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 30% of EtOAc in hexanes) to yield the title compound as a colorless oil.

Example 188 2-((1R,2S,4R,5S)-5-(tert-Butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-yl)isoindoline-1,3-dione

A solution of diethyl azodicarboxylate (2.58 mL, 16.4 mmol) in anhydrous THF (10.0 mL) was added dropwise to a mixture of (1R,2R,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1 ]heptan-2-ol (5.00 g, 13.6 mmol), phthalimide (2.31 g, 15.7 mmol), and triphenyl phosphine (4.11 g, 15.7 mmol) in anhydrous THF (60 mL) at ambient temp. under nitrogen. After stirring for 32 h, the solvents were removed in vacuo. The residue was purified by flash column chromatography (0 to 20% of ethyl acetate in hexanes) to give the title compound as a white solid. MS m/z: 496.3 (M+H)⁺.

Example 189 1-((1R,2S,4R,5S)-5-(tert-Butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-yl)thiourea

To a suspension of 2-((1R,2S,4R,5S)-5-(tert- butyldiphenylsilyloxy)bicyclo[2.2.1]-heptan-2-yl)isoindoline-1,3-dione (4.60 g, 9.28 mmol) in ethanol (anhydrous, 100 mL) was added anhydrous hydrazine (0.44 mL, 13.9 mmol). After refluxing under nitrogen for 3 h, the mixture was cooled to ambient temp. The white solid was removed by filtration, and the filtrate was concentrated in vacuo to give an off-white solid, which was stirred with benzoyl isothiocyanate (1.62 mL, 12.1 mmol) in chloroform (100 mL) at ambient temp. overnight. The reaction mixture was diluted with dichloromethane (50 mL) and the solid was removed by filtration. The filtrate was concentrated to give an off-white solid, which was stirred with potassium carbonate (3.85 g, 27.8 mmol) in methanol (100 mL) at ambient temp. for 30 min. The solvents were removed in vacuo, and the residue was partitioned between EtOAc and water. The organic portion was separated, washed with brine, and conc. in vacuo. The residue was purified by flash column chromatography (0 to 60% of EtOAc in hexanes) to give the title compound as a white solid. MS m/z: 425.2 (M+H)⁺.

Method III

Example 190 5-Isopropyl-5-methyl-2-((1R,2S,4R)-5-oxobicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one

Silica gel 60 (particle size, 0.040-0.063 mm, CAS # 63231-67-4, from EMD Chemical Inc., 2.4 g) was added to a solution of 2-((1R,2S,4R,5S)-5-hydroxybicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (0.709 g, 2.51 mmol) in anhydrous dichloromethane (40 mL). The mixture was cooled to 0° C. Pyridinium chlorochromate (1.08 g, 5.02 mmol) was added, and the reaction mixture was gradually warmed to ambient temperature and stirred overnight. The mixture was diluted with dichloromethane, and filtered through a pad of Celite. The solvents were removed in vacuo and the residue was purified by flash column chromatography (0 to 100% of EtOAc in hexanes) to give the title compound as a tan solid.

Method JJJ

Example 191 2-((1R,2S,4R,5R)-5-Hydroxybicyclo[2.2.1]heptan -2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

To a solution of 5-isopropyl-5-methyl-2-((1R,2S,4R)-5-oxobicyclo[2.2.1]heptan-2-ylamino)thiazol-4(5H)-one (0.380 g, 1.36 mmol) in anhydrous THF (20 mL) was added L-Selectride (1.0 M solution in THF, 4.07 mL, 4.07 mmol) in anhydrous THF at −78° C. under nitrogen. After stirring at −78° C. for 3 h., the reaction was quenched with hydrogen peroxide (35 wt % solution in water, 4 mL) and NaOH (10% aqueous, 7 mL). The mixture was warmed to ambient temp. and then in a 65° C. bath overnight. The volatiles were removed in vacuo. The residue was partitioned between CHCl₃/i-PrOH (v/v=3/1) and brine. The organic portion was separated, dried over MgSO₄, filtered, and conc. in vacuo. The residue was purified by flash column chromatography (0 to 5% of MeOH in EtOAc) to give the title compound as a white solid.

Method KKK

A mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(1-hydroxyethyl)-5-methylthiazol-4(5H)-one (0.560 g, 2.09 mmol) and Dess-Martin periodinane (Aldrich, 1.06 g, 2.50 mmol) in CH₂Cl₂ (10 mL) was stirred at room temperature overnight. Sodium thiosulfate (2 g) was added, followed by the addition of satd. NaHCO₃ (20 mL). The resulting mixture was stirred ambient temp. for 20 min. The crude product was extracted with CH₂Cl₂ (3×100 mL). The extract phase was washed with satd. NaCl, dried over Na₂SO₄, filtered and concentrated in vacuo. Purification by flash column chromatography (silica gel, 0-6% MeOH—CH₂Cl₂) afforded the title compound as light yellow solid.

Method LLL

Example 192 5-(3-Hydroxypropyl)-5-methyl-2-((S)-1-(2-(trifluoromethyl)phenyl)ethylamino)-thiazol-4(5B)-one

The mixture of 5-methyl-5-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-2-((S)-1-(2-(trifluoromethyl)phenyl)ethylamino)thiazol-4(5H)-one (0.810 g, 1.82 mmol) and 4-methylbenzenesulfonic acid (0.0314 g, 0.182 mmol) in 20 mL of methanol was stirred at ambient temp. overnight. The solvents were removed in vacuo, and the residue was partitioned between EtOAc and brine. The organic portion was separated, and conc. in vacuo. The residue was purified by flash column chromatography (0 to 100% of EtOAc in hexanes) to give the title compound as a white solid. MS m/z: 361.1 (M+H)⁺.

Method MMM

Example 193 N-Cyclopropyl-N-(3-(5-methyl-4-oxo-2-((S)-1-(2-(trifluoromethyl)phenyl)-ethylamino)-4,5-dihydrothiazol-5-yl)propyl)furan-3-carboxamide

The mixture of 5-(3-(cyclopropylamino)propyl)-5-methyl-2-((S)-1-(2-(trifluoromethyl)-phenyl)ethylamino)thiazol-4(5H)-one (0.106 g, 0.265 mmol), 3-furoic acid (0.0297 g, 0.265 mmol), TBTU (0.0895 g, 0.279 mmol), and N,N-diisopropylethylamine (0.0555 ml, 0.318 mmol) in DMF (3.0 mL) was stirred at ambient temp. overnight. The mixture was partitioned between EtOAc and Na₂CO₃ (aq), and the combined organic portions were washed with brine. The solvents were removed in vacuo, and the residue was purified by flash column chromatography (0 to 100% of EtOAc in hexanes) to give the title compound as a white solid. MS m/z: 494.1 (M+H)⁺.

The following table of compounds were prepared using the methodologies outlined above.

TABLE 4 Method Mass of Name Spec Structure Prep. 1911729 291

X AA 1911730 271

X AA 1911749 241.2

P X 1911764 307.1

X 1911810 321.1

Y CC 1911818 321.1

Y CC 1911844 337.1

Y CC 1911846 337.1

Y CC 1912021 283.2

P X AA 1912039 341.2

X GG FF 1912052 335

X AA 1912053 269.1

X FF 1912054 360

X 1912074 271.1

X 1912250 331.1

X AA 1913714 299.2

X FF 1913721 303.1

X 1913769 393, 395

M X 1914926 311.1

X FF 1914927 311.1

X FF 1914928 299

X FF 1914934 333

X 1914937 305

X 1914960 293.2

X 1921446 333.1

X CC 1921448 311

X FF 1932739 342

M X 1932740 313

X FF GG 1932757 307.2

X AA 1932820 393

X AA MM 1932829 407

X AA MM 1932899 407, 409

M X AA 1932906 347

M A AA 1932958 339.0

X CC 1932964 307.1

X CC 1932980 283.1

HHH X AA FFF 1933255 281.1

HHH X AA FFF III 1933301 275.2

X 1933431 414.1

X AA 1933439 283.1

HHH X AA FFF III JJJ 1933454 319

M X AA 1933524 315.1

X CC 1933525 351

X AA 1933528 289.2

X AA 1933690 313.0, 315.0

X 1933815 313.0, 315.0

X CC 1933852 333.1

X CC 1933854 333.1

X CC 1933872 387

YY 1933873 346

M X 1933878 396

M X 1933934 372

X ZZ GGG 1933948 313.1

X FF GG 1933950 313.1

X FF GG 1933985 440

YY 1933986 426

YY 1934076 283.1

HHH X AA FFF 1934079 283.1

HHH X AA FFF 1934081 281.1

HHH X AA FFF III 1934082 281.1

HHH X AA FFF III 1934083 283.1

HHH X AA FFF III JJJ 1934084 283.1

HHH X AA FFF III JJJ 1934139 401

X AA 1934291 445.1

X AA 1934329 381.0, 383.0

X CC 1934339 287.1

X FF 1934342 257.1

X 1934379 361.1

X AA LLL 1934463 359.1

X AA LLL III 1934471 328.1

X CC CCC 1934518 360

M X 1934520 410

M X 1934533 354

X ZZ 1934537 360

M X 1934538 360

M X 1934579 494.1

X AA LLL JJ MMM 1934603 309.1

X 1934605 311.1

X GG 1934608 337.1

X FF 1934609 339.1

X FF GG 1934612 500

X AA 1934622 331.1

X 1934705 313

X FF GG 1934706 313

X FF GG 1934707 289

X FF KKK GG 1934708 289

X FF KKK GG 1934709 311

X FF KKK GG 1934710 311

X FF 1934737 345.2

X AA 1934738 269.1

X 1934858 309.1

X CC 1934859 283.1

X AA 1934872 387.0, 389.0

X CC BBB 1934892 311.1

X CC 1934921 394.2

X FF 1934922 396.2

X FF GG 1934972 361.0, 363.0

X AA BBB 1934974 334

X CC BBB CCC 1935213 361

X FF 1935214 363

X FF GG 1935215 442

X AA MM 1935724 386

YY 1935728 412

YY 1935794 341, 343

X 1935795 341.1, 343.1

X 1938535 355.1, 357.1

X AA 1938536 355.1, 357.1

X AA 1938917 241.2

X AA 1938932 372

X ZZ GGG 1938935 372

X ZZ GGG 1938946 456

X AA MM 1938947 493

X AA MM 1938975 376.2

X GG MM 1938978 456.2

X FF 1939109 458.2

X FF GG 1939110 438

X FF GG 1939113 510

X AA MM 1939236 468

X AA MM 1939238 482

X AA MM 1939284 283.1

X AA 1939286 361.0, 363.0

X AA BBB 1939294 396

AAA M X AA EEE 1939308 311.1

X AA LLL 1939309 486.1

X AA LLL JJ MMM 1939311 392.1

X AA LLL JJ 1939315 434.1

X AA LLL JJ MMM 1939317 460.1

X AA LLL JJ MMM 1939320 459.2

X AA LLL JJ MMM 1939475 299.1

X FF 1939595 283.1

X AA 1939597 283.1

X AA 1939600 377, 379

X GG BBB 1939811 494

X AA MM 1939813 478

X AA MM 1939963 319.2

X 1939996 361.0, 363.0

X AA BBB 1939998 361.0, 363.0

X AA BBB 1940062 457

X AA MM 1940064 317

X FF KKK GG 1940065 317

X FF KKK GG 1940104 361.2

X AA 1940113 363

X FF GG 1940114 363

X FF GG 1940117 361

X FF 1940118 361

X FF 1940306 257.2

X AA 1940326 271.1

X AA 1940464 361.2

X AA 1940489 389.1

X FF 1940570 354

X ZZ 1940573 401

X AA 1940576 368

X AA 1940630 386

X AA GGG 1940851 323.2

X FF 1940852 323.2

X FF 1940918 271.2

X AA EEE 1941044 404

X AA 1941045 372

X ZZ GGG 1941046 422

X ZZ GGG 1941081 370

X ZZ 1941082 281.2

X 1941249 327.1

X FF 1941251 361.1

X FF 1941719 257.2

X AA FFF 1941733 323.2

X AA 1941734 388

X ZZ GGG 1941736 354

X ZZ 1944205 372

X ZZ GGG 1944206 359

X YY (step 1) LiAlH₄ 1944316 321.1

O X AA 1944337 283.1

HHH X FFF 1945015 269.1

HHH X FFF 1945077 341.2

X GG FF 1946034 463

X 1946066 299

X FF 1946067 299

X FF 1946068 353.1

X FF 1946069 271.1

X AA 1946070 271.1

X AA 1946076 394

X ZZ 1946082 323.1

HHH X FFF 1946083 283.1

HHH X FFF 1946084 283.1

HHH X FFF 1946117 368

X ZZ 1946119 323.1

X FF 1946120 327.1

X FF 1946121 327.1

X FF 1946122 393

X AA 1946123 323.1

X FF 1946124 412

X ZZ GGG 1946247 386

X ZZ GGG 1946253 257.2

X AA FFF 1946254 257.2

X AA FFF 1946256 257.2

X AA FFF 1946258 257.2

X AA FFF 1948882 327.1

X FF 1948883 339.2

X FF 1948926 387

X ZZ 1948951 353.1

X FF 1948954 339.2

X FF 1948955 339.2

X FF 1949173 271.2

X AA FFF 1949187 283

X FF 1949219 271.2

X AA DDD 1949574 379

X AA 1949578 396

X ZZ 1949627 339.2

X FF 1949628 339.2

X FF 1949683 307

X FF 1949684 371, 373

X FF 1949699 301.1

HHH X FF GG 263.1

HH 229.1

HH 277.2

HH 277.1

HH

The following tables of compounds are encompassed by the present invention and may be prepared by one of the above methodologies.

TABLE 5 Compound Name

(S)-2-((1R,2R,4R)-5- hydroxybicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5-methylthiazol- 4(5H)-one

(S)-2-((1R,2S,4R)-5- hydroxybicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5-methylthiazol- 4(5H)-one

(S)-2-((1R,2S,4R)-6- hydroxybicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5-methylthiazol- 4(5H)-one

(S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan- 2-ylamino)-5-((R)-1-hydroxypropan-2- yl)-5-methylthiazol-4(5H)-one

(S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan- 2-ylamino)-5-((S)-1-hydroxypropan-2- yl)-5-methylthiazol-4(5H)-one

(S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan- 2-ylamino)-5-(2-hydroxypropan-2-yl)-5- methylthiazol-4(5H)-one

(S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan- 2-ylamino)-5-methyl-5-(prop-1-en-2- yl)thiazol-4(5H)-one

(S)-2-((1R,2S,4R)-5- hydroxybicyclo[2.2.1]heptan-2- ylamino)-5-isopropyl-5-methylthiazol- 4(5H)-one

In the table that follows, the variable n is defined as 0-8, the variables R and R₁ and R₂ are independently defined as hydrogen, C₁-C₈ alkyl, C₁-C₈ alkoxy, —NR¹⁰R¹⁰, —S-(C₁-C₈)alkyl, aryl and heterocyclyl; where R¹⁰ independently selected from hydrogen, C₁-C₈ alkyl, aryl-C₁-C₈ alkyl, C₁-C₈ alkoxy, —S-(C₁-C₈)alkyl, heterocyclyl and aryl; and any alkyl, alkoxy, heterocyclyl or aryl moiety may be substituted with one to three substituents selected from -halo, unsubstituted C₁-C₈ alkyl, unsubstituted C₁-C₈ alkoxy, unsubstituted C₁-C₈ thioalkoxy and unsubstituted aryl(C₁-C₄)alkyl.

TABLE 6

2-(cyclooctylamino)-5-isopropyl-5- methylthiazol-4(5H)-one

2-(5-hydroxy-5- (trifluoromethyl)cyclooactylamino)-5- isopropyl-5-methylthiazol-4(5H)-one

2-(5,5-difluorocyclooactylamino)-5- isopropyl-5-methylthiazol-4(5H)-one

2-((S)-8-fluoro-1,2,3,4- tetrahydronaphthalen-1-ylamino)-5-methyl- 5-(trifluoromethyl)thiazol-4(5H)-one

2-((S)-8-chloro-1,2,3,4- tetrahydronaphthalen-1-ylamino)-5-methyl- 5-(trifluoromethyl)thiazol-4(5H)-one

2-((S)-7-chloro-2,3-dihydro-1H-inden-1- ylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)-one

2-((S)-7-fluoro-2,3-dihydro-1H-inden-1- ylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)-one

2-((S)-1-(2-fluoro-6- methylphenyl)ethylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)-one

2-((S)-1-(2-chloro-6- methylphenyl)ethylamino)-5-methyl-5- (trifluoromethyl)thiazol-4(5H)-one

2-((S)-1-(2-chlorophenyl)ethylamino)-5- isopropyl-5-methylthiazol-4(5H)-one

2-((S)-1-(2-ethynylphenyl)ethylamino)-5- isopropyl-5-methylthiazol-4(5H)-one

2-((S)-1-(2-ethynylphenyl)ethylamino)-5- methyl-5-(trifluoromethylthiazol-4(5H)- one

2-((S)-1-(2-chlorophenyl)ethylamino))-8- oxa-1-thia-3-azaspiro[4.5]non-2-ene-4-one

2-((S)-1-(2-bromophenyl)ethylamino))-8- oxa-1-thia-3-azaspiro[4.5]non-2-ene-4-one

2-((S)-1-(2-bromophenyl)ethylamino))-1- thia-3-azaspiro[4.4]non-2-ene-4-one

2-((S)-1-(2-chlorophenyl)ethylamino))-1- thia-3-azaspiro[4.4]non-2-ene-4-one

2-((1S,5R)-6,6- difluorobicyclo[3.1.0]hexan-3-ylamino)-5- isopropyl-5-methylthiazol-4(5H)-one

2-((1S,5R)-6,6- difluorobicyclo[3.1.0]hexan-3-ylamino)-5- methyl-5-(trifluoromethyl)thiazol-4(5H)- one

2-(6,6-difluorobicyclo[3.1.0]hexan-3- ylamino)-1-thia-3-azaspiro[4.4]non-2-ene- 4-one

Preparation of a Pharmaceutical Composition Example 194 Preparation of Tablets

Ingredients mg/tablet 1. Active compound of the invention 10.0 2. Cellulose, microcrystalline 57.0 3. Calcium hydrogen phosphate 15.0 4. Sodium starch glycolate 5.0 5. Silicon dioxide, colloidal 0.25 6. Magnesium stearate 0.75

The active ingredient 1 is mixed with ingredients 2, 3, 4 and 5 for about 10 minutes. The magnesium stearate is then added, and the resultant mixture is mixed for about 5 minutes and compressed into tablet form with or without film-coating.

The present invention is not to be limited in scope by the exemplified aspects which are intended as illustrations of single aspects of the invention. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and accompanying drawings. Such modifications are intended to fall within the scope of the appended claims.

All references cited herein are hereby incorporated by reference in their entirety. 

What is claimed is:
 1. A compound selected from the group consisting of:

or pharmaceutically acceptable salts, tautomers, optical isomers, N-oxides and prodrug forms thereof.
 2. A pharmaceutical formulation comprising a compound according to claim 1 in combination with a pharmaceutically acceptable diluent or carrier.
 3. The pharmaceutical formulation of claim 2, wherein the formulation is formulated for oral delivery.
 4. The pharmaceutical formulation of claim 3, wherein the oral delivery is in the form of a tablet.
 5. A method for the treatment of an 11-β-hydroxysteroid dehydrogenase type 1 enzyme-mediated disorder comprising administering a therapeutically effective amount of the compound of claim 1 to an individual in need thereof, wherein the disorder is selected from diabetes, syndrome X, obesity, glaucoma, hyperlipidemia, hyperglycemia, hyperinsulinemia, hypertension, osteoporosis, dementia, and depression.
 6. A method for the treatment of a medical condition involving delayed or impaired wound healing comprising administering a therapeutically effective amount of the compound of claim 1 to an individual in need thereof.
 7. The method according to claim 6, wherein the medical condition involving delayed or impaired wound healing is diabetes.
 8. The method according to claim 6, wherein the medical condition involving delayed or impaired wound healing is caused by treatment with glucocorticoids.
 9. The method according to claim 6 wherein the medical condition is selected from the group consisting of for the promotion of wound healing in chronic wounds diabetic ulcers, venous ulcers and pressure ulcers.
 10. A method for the treatment of tuberculosis, leprosy, or psoriasis comprising administering a therapeutically effective amount of the compound of claim 1 to an individual in need thereof.
 11. A method for inhibiting a 11-β-hydroxysteroid dehydrogenase type 1 enzyme, which comprises administering to a subject in need of such treatment an effective amount of a compound according to claim
 1. 